Benzoic Acids

<p>2-Amino-6-chlorobenzoic acid is a fine chemical that is used as a reagent or speciality chemical.</p>

<p>Bis(2-ethylbutyl)phthalate (BEBP) is a chemical that has been used in the production of polyvinyl chloride (PVC) plastics, and as a stabilizer for PVC resins. BEBP is found in low levels in human tissue samples and sediments. Levels of BEBP have been measured through gas chromatography-mass spectrometry and liquid chromatography-mass spectroscopy methods. The environmental concentrations of BEBP can be calculated using the linear regression equation. Biota are also exposed to this chemical, which may be due to its use as an additive in certain food packaging materials.</p>

<p>4-Bromo-2-(trifluoromethyl)benzoic acid methyl ester is a versatile building block that can be used to produce complex compounds. It is also an intermediate and a useful scaffold in organic synthesis. This chemical has been used as a research chemical and as a reagent for the production of other chemicals. The compound has CAS number 957207-58-8 and can be obtained from our supplier in high quality, with purity of 99%.</p>

<p>4-Hydroxy-3-iodobenzoic acid is a synthetic retinoid that is used in the synthesis of various other pharmaceutical compounds. It is also an inhibitor of bacterial growth, which may be due to its ability to bind to receptors on the bacterial cell surface. The antibiotic activity of 4-hydroxy-3-iodobenzoic acid has been demonstrated using an in vitro assay with Escherichia coli and Streptococcus pyogenes. 4-Hydroxy-3-iodobenzoic acid has also been shown to have antiestrogen properties when it competes with estradiol for receptor binding sites. This compound binds to the estrogen receptor and blocks its activity, inhibiting estrogen production by the ovaries or from other sources. Structural analysis of 4-hydroxy-3-iodobenzoic acid revealed that this compound has two functional groups: one group that interacts with nitrogen and another that binds to hydrogen or oxygen. These</p>

<p>3-Bromo-4-methoxybenzoic acid is a methyl ester of 3-bromo-4-methoxybenzoic acid. It is used as a reagent in organic synthesis, including the hydrolysis of esters and nitriles to acids and amines respectively. The compound is also used in the synthesis of 3-bromo-4-methoxybenzamide and other bromomethyl benzoates. The trifluoroacetic acid reacts with cuprous cyanide to form ethyl formate and methoxybenzoate, which reacts with thionyl chloride to form the chloride 3-bromo-4-methoxybenzoic acid. This compound can be demethylated by acetaldehyde or alkali metal hydroxides to give methyl formate and methanol. It can also react with acetonitrile to produce 3,3′,3″</p>

<p>3,4,5-Tribromobenzoic acid is a metabolite of 3-indoleacetic acid. It is excreted in the urine and has a phaseolus-like physiological activity. This compound has been found to reduce the number of internodes in plants and increase the number of subjacent nodes. In addition, it has been shown to inhibit abscission (the separation of plant parts) by inhibiting the release of auxin from the upper node. The structural properties of 3,4,5-tribromobenzoic acid are similar to those of benzoic acid and it can be found naturally in some plants. Diversity in this chemical has been found among different species: for example, 2,3,5-triiodobenzoic acid is only present in citrus fruits such as oranges and lemons.</p>

<p>2-Phenoxybenzoic acid is a hydrochloride salt that is used as a reagent in analytical chemistry. It reacts with the carboxylate group of amino acids, proteins, and peptides to form a stable, water-soluble complex. The reaction is typically monitored by measuring the change in optical density at 260 nm. 2-Phenoxybenzoic acid reacts with bcr-abl kinase and colloidal gold to form an insoluble precipitate that can be detected with electron microscopy. This compound also has biological properties such as inhibiting carbonic anhydrase activity and changing the pH of the solution. 2-Phenoxybenzoic acid was originally synthesized from diphenyl ether and phenol (C6H5OH).<br>2-Phenoxybenzoic acid can be converted into 2-(4-nitrophenoxy) benzoic acid by reacting it with sodium nitrite followed by hydrochloric acid</p>

<p>2,5-Dichlorobenzoic acid methyl ester is a synthetic chemical compound that belongs to the class of aryl chlorides. It is soluble in organic solvents and can be polymerized using the vibrational method. 2,5-Dichlorobenzoic acid methyl ester has been shown to inhibit the growth of various bacteria strains by binding to sulfhydryl groups on proteins and inhibiting protein synthesis. This chemical also inhibits the uptake of sulfate ions by inhibiting the enzyme sulfate adenylyltransferase.</p>

<p>2-Methoxy-4-aminobenzoic acid is a solute that can be used in the manufacture of pharmaceuticals. It has a high affinity for receptors and is potentially useful in the treatment of hypertension. 2-Methoxy-4-aminobenzoic acid has been shown to exhibit antihypertensive activity in animals by reducing cardiac output, systemic vascular resistance, and total peripheral resistance. The mechanism of action may be due to its ability to inhibit calcium ion influx into myocardial cells and block voltage-gated potassium channels. This drug also has an acidic pH, which makes it soluble in water. 2-Methoxy-4-aminobenzoic acid is insoluble in organic solvents such as hydrochloric acid or ether, which means it cannot be extracted from aqueous solutions by these solvents.</p>

<p>2,3-Dihydroxybenzoic acid is an antioxidant found in many plants. It has a protective effect against oxidative injury. 2,3-Dihydroxybenzoic acid has been used as a model for the study of infectious diseases and its effects on biological studies. This compound has been shown to prevent the growth of Aerobacter aerogenes and Dinucleotide phosphate. 2,3-Dihydroxybenzoic acid is also used as an ingredient in sephadex g-100 and it acts as an antimicrobial agent that prevents microbial growth in wastewater treatment systems.</p>

<p>3,5-Dihydroxybenzoic acid methyl ester is a potent tyrosinase inhibitor that has been shown to be effective in inhibiting the production of melanin. 3,5-Dihydroxybenzoic acid methyl ester is an active ingredient in skin lightening products and has been shown to be more potent than kojic acid, arbutin and ascorbic acid. The reaction mechanism of 3,5-Dihydroxybenzoic acid methyl ester is stepwise with hydroxybenzoic acid (HBA) being the first substrate. HBA reacts with iron oxides to form a ferric hydroxide intermediate that undergoes gelation reactions with chloride ions. This results in a molecule containing three ether linkages, which are responsible for its inhibitory activity on the enzyme tyrosinase.</p>

<p>2,5-Dichlorobenzoic acid is a hydrogen-bonding agent that interacts with other molecules by forming hydrogen bonds. It reacts with benzoate to form 2,5-dichlorobenzoate, which is an intermediate in the synthesis of phenylbenzene and biphenyl. 2,5-Dichlorobenzoic acid has been shown to inhibit the growth of bacteria such as Stenotrophomonas maltophilia and Pseudomonas aeruginosa. The compound also lowers cholesterol levels in rats and humans.<br>2,5-Dichlorobenzoic acid has a redox potential of -0.25 V and can be used to reduce sodium hydroxide solution or hydroxide solution. This chemical's structure allows it to be taken up by cells through passive diffusion and active transport mechanisms.</p>

<p>3,4-Dimethoxy-2-hydroxybenzoic acid (DMHA) is a potential drug candidate that has been shown to scavenge free radicals and protect against the damage caused by oxidative stress. It has also been found to have heartwood extract-modulating properties, inhibiting the growth of Madagascariensis, Angolensis, and Leukemia cells. DMHA has been shown to be effective in preventing lipid peroxidation and may have dietary benefits for prevention of chronic diseases such as cancer and diabetes. This compound is being investigated as a potential drug for administration by chemometric methods. DMHA was also found to be a potent inhibitor of cyclooxygenase 2 (COX-2), which could make it useful for treating inflammatory conditions.</p>

<p>4,5-Dimethoxy-2-nitrobenzoic acid is a versatile building block and reagent that can be used in research and development as well as for the production of fine chemicals. This compound has been shown to react with amines using the nitration reaction to produce a variety of useful compounds. The synthesis of this compound is not difficult, but requires care and some speciality chemicals. 4,5-Dimethoxy-2-nitrobenzoic acid is also a useful scaffold for complex compounds. It reacts readily with other building blocks to form nitrogen heterocycles and is used in the production of pharmaceuticals and pesticides.</p>

<p>Methyl 4-aminobenzoate is a chemical compound that is used as a fluorescence probe in the study of DNA replication. It can be used to detect the presence of viral RNA in cell culture, and has been shown to inhibit the replication of bacterial RNA. Methyl 4-aminobenzoate binds to guanine residues in DNA and forms an alkyl bond with them. This prevents the binding of other amino acids, which are essential for DNA replication. Methyl 4-aminobenzoate has also been shown to have pharmacokinetic properties that make it useful for intravenous administration and oral administration.</p>

<p>2-Chloro-4-methoxybenzoic acid is a model compound for the screening of acridones, which are a class of compounds with anticancer activity. 2-Chloro-4-methoxybenzoic acid has been shown to inhibit potassium t-butoxide efflux in cancer cells and induce multidrug resistance in cancer cells. Furthermore, it has been shown that 2-Chloro-4-methoxybenzoic acid inhibits mitoxantrone efflux in cancer cells, leading to an increase in mitoxantrone cytotoxicity. This compound is also able to induce a phenotype change from cancerous to normal and can be used as a chemotherapeutic agent against cancers.</p>

<p>2-(4'-Chlorobenzoyl)benzoic acid (2-CBA) is a sulfa drug that inhibits bacterial growth by blocking the synthesis of folic acid. It is also known to be luminescent and can be used in techniques such as luminescent probes. 2-CBA has antibacterial activity and can inhibit bacterial growth in a chromatographic method. 2-CBA is chemically stable and has been shown to have antibacterial properties against gram-positive bacteria, including Bacillus subtilis and Staphylococcus aureus. 2-CBA also has the ability to react with phthalazinone, an inhibitor of glutamine synthetase, which is involved in the production of ATP from ADP. This reaction results in the formation of an unstable intermediate which decomposes into CO2 and benzoic acid.</p>

<p>4-Amino-3-methoxybenzoic acid is an inhibitor of the enzyme hydroxylase. It has been shown to inhibit cancer cell growth in nanomolar concentrations and may be a potential anti-cancer drug candidate. 4-Amino-3-methoxybenzoic acid inhibits the production of 3-methoxy-4-nitrobenzoic acid, which is an intermediate in the biosynthesis of cyclic peptides. This compound also has potent inhibitory activity against active enzymes involved in the biosynthesis of 3-methoxy-4-nitrobenzoic acid, such as hydroxylases, nitroreductases, and methyltransferases.</p>

<p>4-Acetylbenzoic acid is a reactive functional group that is used to synthesize esters and amides. It has been shown to have anticancer activity in vitro, which may be due to the disruption of basic cellular proteins involved in DNA replication. 4-Acetylbenzoic acid is soluble in neutral pH and reacts with nucleophiles such as hydroxide ions or alcohols, forming alcohols or acetates respectively. The reaction mechanism for this compound is nucleophilic attack on the carbonyl carbon, followed by loss of water from the leaving group. Significant cytotoxicity has been observed in vitro at concentrations of 2mM and higher. This effect was particularly pronounced for cells exposed to radiation or treated with 4-acetylbenzoic acid before being exposed to radiation.</p>

<p>Gallic acid anhydrous is a compound that is found in plants and has antioxidant properties. Gallic acid anhydrous can be used as a model system for the study of electrochemical impedance spectroscopy. It has shown to have anti-cancer activity in vitro, but not in vivo, against squamous carcinoma cells. In addition, gallic acid anhydrous has been shown to inhibit oral pathogens and to scavenge anion radicals. Gallic acid anhydrous may have structural similarities to procyanidin B4, which is important for its antioxidant activity.</p>

<p>Organic anion transporter inhibitor; pannexin 1 channel inhibitor</p>

<p>2-Methoxy-3-methylbenzoic acid is a methoxy methyl, benzyl, methyl ether that can be used as a reagent in organic chemistry. It is an intermediate in the synthesis of phthalic anhydride and in the production of esters and quinones. 2-Methoxy-3-methylbenzoic acid is also used to produce potassium t-butoxide, which can be used for the synthesis of new types of reagents for organic synthesis. The chemical reacts with potassium hydroxide or potassium t-butoxide to form potassium 2-methoxy 3-methyl benzoate, which is soluble in water. This compound can also be produced from methoxy methyl benzyl chloride by reacting it with either potassium or sodium hydroxide.</p>

<p>2,3,4-Trimethoxybenzoic acid is a molecule that has been shown to stimulate epidermal growth. It is a methylating agent that can be used to produce 2-hydroxybenzoic acid from protocatechuic acid. The hydroxy group on the 2,3,4-trimethoxybenzoic acid binds to the chloride ion in the protocatechuic acid and removes it from the molecule. This reaction mechanism is supported by x-ray crystal structures of protocatechuic acid and 2,3,4-trimethoxybenzoic acid.</p>

<p>Ethyl 4-bromobenzoate is a halide that can be synthesized by the cross-coupling reaction with an aryl halide and a boronic acid. This synthesis has been used successfully to prepare benzoates, which are generally more difficult to synthesize than boronic acids. The coupling reaction of ethyl 4-bromobenzoate with an aryl halide and a boronic acid in the presence of copper as catalyst yields ethyl 4-bromobenzoate in high yield. A synergistic interaction occurs between the two reagents, leading to significant cytotoxicity in vitro. This property may be due to the light emission from this compound when it is exposed to ultraviolet light. Ethyl 4-bromobenzoate is also able to inhibit aerobic glycolysis and cancer cell growth in vitro through its ability to inhibit the activity of phosphofructokinase 1 (PFK1</p>

<p>3-Formyl-4-hydroxybenzoic acid is a synthetic compound with anticancer activity. It is an azobenzene that has been shown to have photocatalytic activity. 3-Formyl-4-hydroxybenzoic acid has a carboxylate functional group and the ethyl ester functional group. The anticancer activity of this compound may be due to hydrogen bonding interactions, as well as its ability to cause DNA damage in cells by photolysis and its antiviral potency.</p>

<p>Methyl 4,5-dimethoxy-3-hydroxybenzoate is a synthetic chemical that inhibits the enzyme tectorigenin reductase. Tectorigenin reductase is responsible for the production of tectorigenin, a phytoestrogen found in plants such as china. Methyl 4,5-dimethoxy-3-hydroxybenzoate was shown to inhibit the activity of platelets from human blood and has been studied for its pharmacological properties. The thermodynamic and kinetic parameters of methyl 4,5-dimethoxy-3-hydroxybenzoate have been determined using gas chromatography - mass spectrometry (GC–MS) and nuclear magnetic resonance (NMR) spectroscopy. It exists as both an enantiomeric mixture and racemic mixture.</p>

<p>2-Chloro-4-methylsulfonylbenzoic acid is a chlorinating agent that can be used to produce triketones from ketones. It is usually used as a hydrogen peroxide scavenger and a chlorinating agent in the food industry. 2-Chloro-4-methylsulfonylbenzoic acid can also be used to produce glyphosate, phosphoric acid solution, and chloride. The chlorinating property of this compound is due to its ability to form hypochlorous acid when it reacts with water. This reaction produces hypochlorite ions that are active against microorganisms by disrupting the cell membrane. 2-Chloro-4-methylsulfonylbenzoic acid can react with organic solvents such as carbon tetrachloride and optimizes the introduction of chlorine into organic compounds.</p>

<p>o-Sulfobenzoic acid anhydride is a chemical that belongs to the class of inorganic acids. It is a white crystalline solid with a melting point of 107°C and can be found in its pure form or as sodium salts. o-Sulfobenzoic acid anhydride is stable when exposed to light and can be used in detergent compositions. It also has pharmacokinetic properties, which are affected by the presence of cationic polymers. This chemical is metabolized by microorganisms through hydrogen bonding interactions and has been shown to have antimicrobial activity against infectious bacteria, such as erythromycin-resistant strains of Staphylococcus aureus and Mycobacterium tuberculosis.</p>

<p>2,4-Dihydroxy-3-methylbenzoic acid (2,4-DMB) is a potent compound that has been shown to have chemotherapeutic properties. It is a DNA repair agent that also inhibits the activity of topoisomerase II and DNA polymerase III. 2,4-DMB can be used in the treatment of radiation and ionizing radiation induced cancers. The pharmacophore of 2,4-DMB has been identified as being composed of three hydrophobic regions and one hydrophilic region. This pharmacophore has been used to design other potent compounds with similar activity against cancer cells.</p>

<p>Methyl 4-acetylbenzoate is a synthetic compound that can be used for the synthesis of imatinib and other pharmaceuticals. It is an effective method for the synthesis of butyric acid with high enantiomeric purity. The cross-coupling reaction was first reported by Suzuki in 1979, which has been widely applied to organic synthesis because it is efficient and produces simple byproducts. This reaction has also been used in the synthesis of model compounds and natural products, as well as in environmental pollution studies.</p>

<p>2,4-Dimethoxybenzoic acid is a phenolic compound that has been shown to bind to the ferrocene carboxylate of protocatechuic acid. The resulting complex was shown to be able to react with chloride ions in an acylation reaction. The kinetic study showed that the rate of reaction increased with increasing concentration of 2,4-dimethoxybenzoic acid. The protonation of 2,4-dimethoxybenzoic acid also increases its ability to react with chloride ions. This acidic compound can also react with amines and other compounds containing nitrogen in a similar manner as acetic anhydride. Addition of alkali hydrolysis may cause the cleavage of the hydrogen bond between 2,4-dimethoxybenzoic acid and protocatechuic acid, releasing 2,4-dimethoxybenzoic acid and protocatechuic acid.</p>

<p>3-Hydroxybenzoic acid is a ferroelectric compound that can be found in water vapor, plants, and bacteria. It has been shown to have structural properties that are very similar to those of p-hydroxybenzoic acid. The redox potential of 3-hydroxybenzoic acid is around -0.8 volts versus the standard hydrogen electrode (p-hydroxybenzoic acid is -1.2 volts). 3-Hydroxybenzoic acid has been shown to inhibit some bacterial enzymes such as esterase and transaminase, but not others such as dehydrogenase or oxidoreductase. It also shows activity against fungal enzymes such as aminopeptidases and serine proteases. The compound can exist in two forms: the metastable form or a stable form. The metastable form can be obtained by crystallizing the compound from a solution containing copper chloride or x-ray diffraction data from wild type strains</p>

<p>Ethyl 2-methoxybenzoate is a colorless liquid that is used as an intermediate in the synthesis of other organic compounds. It has been shown to be an effective insect repellent, with an LD50 of 14 mg/kg. This compound also has a high affinity for protonated amines and amino acids, which may account for its adsorption to riparia. Ethyl 2-methoxybenzoate is biosynthesized from monoketones and monohydric alcohols. The hydroxyl group on the benzoic acid moiety reacts with methyl anthranilate to produce ethyl 2-methoxybenzoate.</p>

<p>2-Methyl-6-nitrobenzoic acid is a yellow needle solid that is soluble in organic solvents. It is used as a reagent to prepare other chemicals and has been shown to react with sodium hydrogen sulfate, chloride, and sulfuric acid to form 2-methyl-6-nitrobenzenesulfonic acid. The mixture of 2-methyl-6-nitrobenzoic acid and sodium hydrogen sulfate reacts violently with chlorine gas or argon. This reaction solution can be evaporated by heating at atmospheric pressure or under vacuum, leaving 2-methyl-6-nitrobenzenesulfonic acid behind. 2MBA can also be purified by filtration or recrystallization from a suitable solvent such as chloroform or ether.</p>

<p>4-Mercaptobenzoic acid is a receptor antagonist that binds to the benzodiazepine site of the GABAA receptor and blocks the action of GABA. This drug has been shown to be useful in tissue culture studies, where it inhibits the growth of cells by interfering with cell division. 4-Mercaptobenzoic acid has also been shown to inhibit sodium citrate uptake into human red blood cells in vitro, which may be due to its ability to bind with hydrogen bonding interactions or ionic interactions. 4-Mercaptobenzoic acid enhances pluronic p123 and fetal bovine serum as a substrate for tissue culture cells, which may be due to its ability to inhibit inhibitor molecules.</p>

<p>2-Isopropylbenzoic acid is a fine chemical that belongs to the group of aromatic compounds and has the molecular formula C8H10O2. This compound is used in research as an intermediate for organic synthesis, such as the production of pharmaceuticals. 2-Isopropylbenzoic acid is also a versatile building block for complex molecules, such as dyes and fragrances. It can be used as a reagent or speciality chemical in research and development, such as in polymer chemistry. 2-Isopropylbenzoic acid can be used as a reaction component for synthesis of other chemicals, such as pharmaceuticals. As an intermediate, it can be used in the production of synthetic drugs and other bioactive molecules that are difficult to synthesize by other means due to its high quality.</p>

<p>Gentisic acid sodium salt hydrate is a benzoate that is used as a diagnostic agent in the study of inflammatory bowel disease. Gentisic acid sodium salt hydrate is a sodium salt of gentisic acid and has been shown to have anti-inflammatory properties. It is used as a stabilizer for solid dispersions, such as capsules, tablets, and granules. Gentisic acid sodium salt hydrate also has the ability to prevent degradation of certain drugs by hydrolysis or oxidation. Gentisic acid sodium salt hydrate can be synthesized from 2,6-dihydroxybenzoic acid (2,6-DHB) and hippuric acid.</p>

<p>2,4-Diaminobenzoic acid dihydrochloride is a versatile building block for complex compounds. This compound can be used as a research chemical and is also a reagent and speciality chemical. 2,4-Diaminobenzoic acid dihydrochloride has been used in the synthesis of many useful compounds, including pharmaceuticals and agrochemicals. It is also an intermediate in the synthesis of some pharmaceuticals and agrochemicals. 2,4-Diaminobenzoic acid dihydrochloride can be used as a scaffold to produce new molecules that are potentially useful as drugs or other chemicals.</p>

<p>3-Amino-2-hydroxybenzoic acid (AAHB) is a nonsteroidal anti-inflammatory drug that belongs to the group of pharmaceutical preparations. It inhibits the enzyme dehydroascorbate reductase, which is involved in the production of hydrogen peroxide and other reactive oxygen species by phagocytes. Hydrogen peroxide and other reactive oxygen species can cause DNA damage and lead to cancer development. AAHB may also have antimicrobial effects, as it has been shown to inhibit bacterial growth and cell adhesion. AAHB interacts with fatty acids in a similar manner as aspirin does, but with a lower potency. It has been shown to inhibit prostaglandin synthesis by inhibiting lipoxygenase activity. The binding of AAHB at these sites prevents the formation of arachidonic acid from linoleic acid and blocks the conversion of arachidonic acid into prostaglandin H2 (PGH2).</p>

<p>Ethyl 3,5-dichloro-4-aminobenzoate is a benzyl amine that has been shown to be an effective inhibitor of nitrile synthesis. It is used as a precursor in the production of dyes and pharmaceuticals. Ethyl 3,5-dichloro-4-aminobenzoate is stable in acidic and alkaline solutions, but decomposes when heated or exposed to cyanide ion. This compound can also react with ethylene diamine to form 2,4-diaminoanisole.</p>

<p>2-Amino-5-methoxybenzoic acid is a useful chemical that can be used as a building block for the synthesis of more complex compounds. It has been used in the synthesis of novel pharmaceuticals and agrochemicals, as well as research chemicals. 2-Amino-5-methoxybenzoic acid is a high quality reagent that can be used in the production of fine chemicals and other specialty chemicals.</p>

<p>Salicylic acid is a weak organic acid that is used as a plant hormone. It has been shown to have enzyme activities that may be involved in the regulation of glycol ether metabolism, photosynthetic activity, p-hydroxybenzoic acid biosynthesis and nutrient solution. Salicylic acid also inhibits nitrite ion production by reacting with acetylsalicylic, which is an inhibitor of the enzyme nitric oxide synthase. Salicylic acid may inhibit transcriptional regulation by steric interactions with DNA or by binding to regulatory proteins. The structural analysis of salicylic acid shows an intramolecular hydrogen bond between the hydroxyl group and carbonyl group which could lead to enzyme inhibition.</p>

<p>Methyl 3-amino-4-chlorobenzoate is an analog of 3-amino-4-chlorobenzoic acid. It is a multidrug that can cross the blood brain barrier and has been shown to have cytotoxic activity in vitro. Methyl 3-amino-4-chlorobenzoate has been postulated as a possible organometallic compound and may be synthesized through a chemical diversity approach. The chloride ion, which is present in methyl 3-amino-4-chlorobenzoate, has been shown to decrease the toxicity of nitrobenzoic acid, making this compound resistant to nitrosation reactions.</p>

<p>Ethyl 3-hydroxybenzoate is a preservative that has been shown to be effective against a variety of microorganisms, including gram-positive and gram-negative bacteria. It has been shown to bind with iron, which prevents it from interacting with tyrosinase, an enzyme necessary for the production of melanin. Ethyl 3-hydroxybenzoate also inhibits the activity of benzodiazepine receptor, which reduces the effects of benzodiazepines in the brain. This compound is used in some cosmetics as an antimicrobial agent and cosmetic preservative. The molecular descriptors for this compound are: Molecular Weight=165.07; Log P=0.5; H-bond acceptor count=3; H-bond donor count=2; rotatable bond count=2; hydrogen bond acceptor count=1; hydrogen bond donor count=2; polar surface area=79.90 Å2</p>

<p>4-(Ethenylsulfonyl)benzoic acid 2,5-dioxo-1-pyrrolidinyl ester is a fine chemical that is a useful scaffold for the synthesis of complex compounds. It can be used as a versatile building block in the production of research chemicals and pharmaceuticals, as well as a reaction component in speciality chemicals. The CAS Number for 4-(Ethenylsulfonyl)benzoic acid 2,5-dioxo-1-pyrrolidinyl ester is 343934-41-8.</p>

<p>3,6-Dichloro-2-hydroxy benzoic acid is a reactive compound that is used as an intermediate in the synthesis of organic compounds. It reacts with the chlorine atom to form a diazonium salt. The diazonium salt then undergoes demethylation, which allows it to be converted into various products such as 3,5-dichloro-2-hydroxybenzoic acid or 2,4-dichloro-3,5-dimethoxybenzoic acid. 3,6-Dichloro-2-hydroxy benzoic acid is a strong base and can react with any acidic compounds present in the reaction vessel. This product has been shown to be effective for wastewater treatment by converting organic compounds into less harmful compounds.</p>

<p>2,4,6-Trimethoxybenzoic acid (TMB) is a monomer that belongs to the class of organic compounds known as phenols. It can undergo dehydrogenation reactions with nitroethane in the presence of trifluoroacetic acid and catalytic amounts of hydrogen gas. TMB has been shown to interact with an allyl group in other molecules. The reaction system was studied under different flow rates and was found to be best described by an isotherm equation.</p>

<p>Methyl 4-(N-methylamino)benzoate is a substance that inhibits the enzyme DPP-4, which is involved in blood glucose regulation. It has been shown to be effective against certain types of cancer and impurities that may be present in the drug. Methyl 4-(N-methylamino)benzoate is an acidic compound with molecular descriptors that include acidic and amines. This compound also has genotoxic impurities, such as benzofurans, which may affect its efficacy.</p>

<p>Methyl 3,5-dibromo-4-methylbenzoate is a versatile building block that can be used as a reagent or a speciality chemical. It is a high quality compound with many applications in research and synthesis. Methyl 3,5-dibromo-4-methylbenzoate is an intermediate in the manufacturing of polymers and pharmaceuticals. It is also a reaction component for the preparation of complex compounds, such as methyl 3,5-dimethoxybenzoate. Methyl 3,5-dibromo-4-methylbenzoate has been shown to be useful as a scaffold for the synthesis of novel compounds.</p>

<p>Intermediate in the synthesis of canagliflozin</p>

<p>Please enquire for more information about 2-Amino-5-iodobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Hydroxy-2-methoxybenzoic acid (3HMB) is a phenolic compound that is found in the heartwood of Eucalyptus trees, fruits such as apples and cherries, and some vegetables. 3HMB has been shown to inhibit tumor necrosis factor-α (TNF-α) production by proinflammatory cytokines such as IL-1β and IL-6, which are produced by cells in response to infection or tissue injury. 3HMB also inhibits the activity of tyrosol oxygenase, which converts tyrosol to vanillic acid. Vanillic acid can be converted into vanillin, an important precursor for the synthesis of pigments that give fruits their color. 3HMB has been shown to inhibit the growth of cancer cells in vitro.</p>

<p>N-Acetyl-4-aminosalicylic acid is an active site directed probe for the detection of salicylic acid. It has a fluorescence emission maximum at 370 nm and a fluorescence quantum yield of 0.93. N-Acetyl-4-aminosalicylic acid can be used to analyze samples, such as wastewater and human urine, which contain salicylic acid. The probe is protonated in the presence of salicylic acid and then binds to the acceptor in the sample with a bimodal distribution. The fluorescence resonance energy transfer (FRET) process between the donor and acceptor leads to an increase in fluorescence intensity that can be detected by electrophoresis methods. This probe also has a conformational change when it binds to its target, which allows for easy separation from other components in the sample by size exclusion chromatography.</p>

<p>2-(Bromomethyl)benzoic acid is a functional group that can be found in many organic compounds. It is a derivative of phthalic acid and has some similar properties, including the ability to form micelles and radical species. 2-(Bromomethyl)benzoic acid has been shown to react with carbon tetrachloride or terephthalic acid to produce peroxides. This reaction is initiated by oxidation of the carbon-carbon double bond, which produces a radical pair that reacts with oxygen in the air to form radicals that are stabilized by resonance. 2-(Bromomethyl)benzoic acid also reacts with an inorganic base such as sodium hydroxide or potassium hydroxide to produce bromine gas and water.</p>

<p>Ethyl 4-chlorobenzoate is an organic compound that is a colorless liquid with a sweet odor. It has been shown to be genotoxic in the presence of impurities such as palladium-catalyzed coupling and hemolytic activity. The structure of ethyl 4-chlorobenzoate can be determined by spectrometry analyses, which show that it contains an isopropyl group and an ethyl ester group. Ethyl 4-chlorobenzoate can be synthesized efficiently using the cross-coupling reaction between chlorides and aryl halides. This synthesis follows the same mechanism as the palladium catalyzed coupling reaction, but uses chloride ions instead of palladium complexes, which are more readily available.</p>

<p>3-Cyanobenzoic acid is a chemical intermediate that is used to synthesize 3-cyanobenzamide. It is also a byproduct of the synthesis of benzonitrile and can be found in metal surface residues and environmental pollution. The molecule has two functional groups, one electron withdrawing and one electron donating, which are necessary for its stability. This compound can be found in high concentrations when it reacts with metal surfaces or organic solvents. 3-Cyanobenzamide was synthesized from 3-cyanobenzoic acid as an amide, which has been shown to have antimicrobial properties against Gram-positive bacteria such as Staphylococcus aureus, Streptococcus pyogenes and Enterococcus faecalis.</p>

<p>Methyl 5-chlorosalicylate is a chemical compound with the molecular formula CHClO. It is a colorless liquid that has a minty odor. Methyl 5-chlorosalicylate is used in organic chemistry as an intermediate to synthesize other compounds, and it can be used in the synthesis of β-cell receptor antagonists. This drug is an analog of salicylic acid and its anti-inflammatory effects are due to the inhibition of chloride channels on macrophages. The drug's neutralizing properties have been shown by experiments with neutralizing antibody levels at physiological levels, which blocks viral replication and prevents cell damage by free radicals.</p>

<p>4-Amino-3-hydroxybenzoic acid is a small molecule that has been shown to inhibit the activity of epidermal growth factor receptor (EGFR) and human epidermal growth factor (HER2). It is also an inhibitor of cytochrome P450 enzymes, which are involved in the metabolism of drugs. 4-Amino-3-hydroxybenzoic acid is used in vitro as an antifungal agent for Candida albicans and other pathogenic fungi. This drug inhibits the growth of cancer cells by binding to specific cell surface receptors, causing them to detach from their surroundings and die. 4-Amino-3-hydroxybenzoic acid may have potential as a drug for treating metastatic colorectal cancer. The mechanism of action is not yet fully understood but it may be related to the inhibition of intermolecular hydrogen bonding and water permeability.</p>

<p>Ethyl 4-nitrobenzoate is a compound that is used to synthesize other drugs, such as erythromycin. It is also an intermediate in the synthesis of some pesticides and dyes. The second-order rate constant for the reaction of ethyl 4-nitrobenzoate with phosphotungstic acid has been measured at 0.058/min at 25°C. This reaction is catalyzed by recombinant cytochrome P450 (P450) enzymes from human liver preparations and cationic surfactants such as nitrobenzene or sodium carbonate, which are known to form hydrogen bonds with the protonated nitrogen atom on the aromatic ring of ethyl 4-nitrobenzoate. Ethyl 4-nitrobenzoate is also used clinically to treat gastric ulcers, although it can be toxic if taken in large doses or over a long period of time.</p>

<p>3,5-Dibromo-2-anisic acid is a short chain dodecyl amine with the chemical formula CH2Br2C6H4N. It is an active compound that has been shown to have nematicidal activity and also shows high activity against saprophytes. 3,5-Dibromo-2-anisic acid is synthesized by reacting chlorine with salicylaldehyde in the presence of a base. The compound is used in the synthesis of various other organic compounds such as amides and amines.</p>

<p>4-Aminomethylbenzoic acid (4AMBA) is a metabolite that is formed from the amino acid methionine. It has been shown to inhibit the growth of prostate cancer cells in vitro and in vivo. 4-Aminomethylbenzoic acid inhibits the activity of polymerase chain reaction (PCR), which is an enzyme that catalyzes DNA replication. The hydroxyl group on 4-aminomethylbenzoic acid reacts with one of the phosphate groups on DNA, forming a covalent bond and inhibiting DNA synthesis. This inhibition occurs at the step called initiation, where DNA synthesis begins by binding of RNA polymerase to a specific sequence of DNA. In addition, 4-aminomethylbenzoic acid also inhibits the activity of x-ray diffraction data, which is an enzyme that catalyzes RNA transcription. Histological analysis shows that 4-aminomethylbenzoic acid causes congestive heart</p>

<p>Alpha-Sulfophenylacetic acid is a high quality reagent that is useful as an intermediate in the synthesis of complex compounds. It is also a fine chemical that can be used as a building block for the synthesis of speciality chemicals and research chemicals. Alpha-sulfophenylacetic acid is a versatile building block for reactions involving organic synthesis, and can be used as a reaction component to produce dyes, pharmaceuticals, pesticides, and herbicides.</p>

<p>4-Dimethylaminobenzoic acid is a cationic surfactant that is used in analytical chemistry to measure the proton concentration. It reacts with protons and forms a positively charged ion. 4-Dimethylaminobenzoic acid can be used in experimental models to study the effects of protonation on cell growth and metabolism. Research has found that 4-dimethylaminobenzoic acid can be used as a growth factor by stimulating the production of protein, DNA, and RNA in cells.<br>4-Dimethylaminobenzoic acid is used as an ingredient in some skin care products because it has been shown to have anti-inflammatory properties.</p>

<p>Dietary polyphenol</p>

<p>2,6-Dihydroxy-4-methylbenzoic acid is a phenolic compound that has been shown to have significant cytotoxicity against cancer cells and may be used in the treatment of various cancers. It is also an endophytic fungus that has been found to produce significant desorption of chloride ions from soil. This compound can also be synthesized by reacting 2,6-dihydroxyphenylacetic acid with methyl iodide or methyl bromide. The reaction system for this synthesis includes concentrated hydrochloric acid, zinc dust, and ethyl acetate. The reaction solution was crystallized in the form of a white solid and the crystals were analyzed by X-ray crystallography to determine their structure. Photocatalytic activity was observed when using 2,6-dihydroxy-4-methylbenzoic acid as an electron donor in a reaction system containing titanium dioxide and hydrogen peroxide as an electron acceptor.</p>

<p>5-Amino-2-nitrobenzoic acid is a useful chemical building block that is used in the synthesis of complex compounds and useful scaffolds.</p>

<p>3,5-Dichloro-2-methoxybenzoic acid (3,5-DMB) is a diphenyl ether with a pharmacokinetic half-life of about 3 hours. It has two isomers: the cis and trans forms. The cis isomer is more active than the trans form. The cis isomer has been shown to be effective in treatments for amine oxidase inhibitors and short-chain fatty acids. It also has growth regulator properties that are used in treatments for psoriasis and acne. 3,5-DMB inhibits bacterial growth by binding to the enzyme dioxygenase, which catalyzes the conversion of 4-hydroxybenzoic acid into 4-hydroxyphenylpyruvic acid; this prevents the production of catecholamines and subsequent cell proliferation. This drug binds to apical membranes in the intestine by attaching to sulfhydryl groups on proteins involved in transport processes, preventing uptake</p>

<p>Methyl 4-amino-2-methyl benzoate is a fine chemical that can be used as a building block for research chemicals, pharmaceuticals, and speciality chemicals. Methyl 4-amino-2-methyl benzoate is a versatile building block in organic synthesis because it can be used as a reaction component and intermediate to synthesize other compounds. This compound is also an excellent scaffold for the synthesis of complex compounds, making it a useful intermediate for organic chemistry. Methyl 4-amino-2-methyl benzoate has CAS No. 6933-47-7 and is soluble in organic solvents such as dichloromethane, chloroform, ether, or acetone.</p>

<p>2-Hydroxy-6-methylbenzoic acid is a natural product that is synthesized by the enzyme p. pastoris. It is a member of the polyketide class of compounds and has shown to have physiological effects such as anti-inflammatory and antioxidant properties. 2-Hydroxy-6-methylbenzoic acid also has been shown to inhibit ATP binding cassette transporter (ABC) proteins, which are involved in drug resistance, from transporting drugs out of cells, making it an attractive candidate for drug discovery.</p>

<p>Iso-propyl 4-aminobenzoate is a chemical intermediate that belongs to the group of aminobenzoates. It can be synthesized by reacting isopropanol with 4-aminobenzoic acid in the presence of an acid catalyst. Iso-propyl 4-aminobenzoate has been used as a chromatographic stationary phase and as a component in the validation of impurities, which are genotoxic. Iso-propyl 4-aminobenzoate is not carcinogenic and has been shown to have a linear regression analysis with pharmacokinetic study data, which was based on plates.</p>

<p>2-Nitrobenzoic acid is a diagnostic chemical that has been used for the detection of epidermal growth factor. It also has therapeutic properties, and has been used to treat infectious diseases and autoimmune diseases. 2-Nitrobenzoic acid is an organic compound that contains two nitro groups, which are connected to a benzene ring by two carbon chains. The molecule also contains two aldehyde groups, which are connected to the benzene ring by one carbon chain each. 2-Nitrobenzoic acid is a white crystalline solid with a melting point of 118°C and boiling point of 310°C. It is soluble in water and alcohols, but insoluble in ethers or chloroform.<br>2-Nitrobenzoic acid can be synthesized from nitric acid and benzoic acid. This reaction produces enough heat to ignite the mixture if it's not cooled down first.</p>

<p>2,4,6-Trimethylbenzoic acid is a molecule that belongs to the class of carboxylates. It has been shown to exhibit anticarcinogenic properties in patients with cervical cancer. 2,4,6-Trimethylbenzoic acid inhibits the growth of cervical cancer cells by blocking the activation of ferrocenecarboxylic acid (FCCA). This compound also blocks the activity of hydrogen bond and nitrogen atoms that are essential for cell division and development. 2,4,6-Trimethylbenzoic acid is used as an intermediate in the production of ferrocene derivatives. It can be used for acylation reactions with aromatic or aliphatic amines under acidic conditions.</p>

<p>Isopropyl 4-hydroxybenzoate is a preservative that is used in cosmetics, pharmaceuticals, and other household products. It can be found in a wide range of products, including moisturizers, shampoos, conditioners, hair sprays, sunscreens, skin lotions and creams. Isopropyl 4-hydroxybenzoate has been shown to inhibit the growth of bacteria by binding to their cell walls. This compound also has been shown to have an antimicrobial effect against fungi and yeast in vitro assays. A number of toxicological studies have been conducted on this compound with no observed adverse effects on animals at doses up to 2,000 mg/kg body weight. The activity index for this compound is low; therefore it does not appear to be carcinogenic or mutagenic. Analytical methods for quantifying this preservative are available in the literature.</p>

<p>4-Aminohippuric acid (4-AHA) is a substance that is used as an analytical tool to measure the amount of inulin in the blood. It is injected intravenously, and the 4-aminohippuric acid enters cells via facilitated transport. In cells, 4-aminohippuric acid binds to pyrazinoic acid to form a fluorescent product that can be detected by a spectrophotometer. This test has been used to study the role of various compounds in the angiotensin system and their effect on renal function.</p>

<p>5,6-Dichlorovanillic acid is a high quality, versatile molecule that can be used as a reagent in organic synthesis or as a building block for the synthesis of complex compounds. It has many useful properties, such as being a fine chemical and research chemicals. 5,6-Dichlorovanillic acid is also a speciality chemical with versatile uses in building blocks or reaction components.</p>

<p>3,5-Dihydroxy-4-methylbenzoic acid methyl ester is a fine chemical that is used as a versatile building block in the synthesis of pharmaceuticals, agrochemicals and other chemicals. It can be used as an intermediate in the synthesis of organic compounds and research chemicals. This compound is also used as a reaction component in organic syntheses and is often found in speciality chemicals. 3,5-Dihydroxy-4-methylbenzoic acid methyl ester is soluble in most solvents and has high purity. It is a complex compound that can be used as a useful building block or reagent for many different reactions.</p>

<p>5-Amino-2-chlorobenzoic acid is a carboxylate that has antiproliferative effects. It is synthesized through the reaction of morpholine and malonic acid. 5-Amino-2-chlorobenzoic acid has been shown to have an optimal reaction with UV light, which may be due to its structure activity relationship with other carboxylates. It also has a high affinity for metal ions such as magnesium and chloride, which are thought to be important in cancer cell proliferation. 5-Amino-2-chlorobenzoic acid can be used in analytical methods because it is soluble in water and can be obtained through gravimetric analysis.</p>

<p>5-Amino-2-nitrobenzoic acid is an organic compound that belongs to the class of versatile building block. It is a white solid that has been used as a research chemical, reagent, and specialty chemical for the synthesis of complex compounds and pharmaceuticals. 5-Amino-2-nitrobenzoic acid is also known as 2-amino-5-chlorobenzoic acid (ACBA). It is soluble in water, but insoluble in ethanol. The CAS number for this chemical is 13280-60-9.</p>

<p>Methyl 4-fluorobenzoate is a potent inhibitor of human cancer cells. It inhibits tyrosine kinases by binding to an imidazole group and forms a ruthenium complex in the presence of sodium carbonate. Methyl 4-fluorobenzoate has shown inhibitory activity against the amination reaction catalyzed by sulfoxide reductase, which is important for the synthesis of nucleic acids. This inhibition may be due to its ability to reduce oxidized species of thiols, sulfoxides, and disulfides. Further studies are needed to elucidate the mechanism by which methyl 4-fluorobenzoate interacts with redox potentials and functional theory.</p>

<p>2,6-Dimethylbenzoic acid is a colorless solid that has a molecular weight of 162.2 g/mol and an empirical formula of C7H8O2. It has a melting point of about 82 degrees Celsius and a boiling point of about 315 degrees Celsius. 2,6-Dimethylbenzoic acid is soluble in water at 100 degrees Celsius. It has been shown to act as a potent antagonist for the muscarinic acetylcholine receptors. This compound also has basic properties due to its hydrogen bonding interactions with proteins and other molecules. 2,6-Dimethylbenzoic acid has been shown to be efficient in supramolecular chemistry because it is electron deficient and contains thermodynamic functional groups such as carboxylic acids and alcohols.</p>

<p>3-Hydroxy-2,4,6-triiodobenzoic acid (3HITBA) is a molecule that is found in the urine of patients with chronic kidney disease. It is present in group P2 of the periodic table. 3HITBA has been demonstrated to have anti-inflammatory properties and may be useful for the treatment of inflammatory diseases. 3HITBA has been shown to inhibit cancer cell growth by inhibiting DNA synthesis and protein synthesis. This molecule also has fluorescence properties and can be used to detect biological fluids such as blood or urine. The structural analysis of this molecule reveals that it contains intramolecular hydrogen bonds, which are important for its stability and activity.</p>