Acidi benzoici

2-Chloro-3,5-dihydroxybenzoic acid (2C3HB) is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It is also used as a reagent for the production of pharmaceuticals and other chemicals. 2C3HB has been shown to be an important reaction component for the synthesis of drugs such as methotrexate and 6-fluoro-3-indoxyl-beta-D-galactopyranoside. This compound has a high quality and can be used as a building block in chemical reactions with other compounds.

<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>3,5-Dimethylbenzoic acid is a carboxylic acid that is a member of the 3-carboxybenzenesulfonic acid family. The molecule is formed by the reaction of sodium carbonate with benzene in the presence of water. The compound has a redox potential that is close to zero, which makes it a reducing agent and an excellent hydrogen donor. The compound is soluble in water and has been shown to inhibit plant growth as well as promote plant growth by acting as a growth regulator. This molecule has also been shown to be fluorescent.</p>

3,4-Dihydroxy-5-methoxybenzoic acid is a natural phenolic compound found in many plants. It has been shown to inhibit the growth of cancer cells and can be used as a chemopreventive agent for cancer treatment. 3,4-Dihydroxy-5-methoxybenzoic acid is metabolized by the liver into 3,4-dihydroxyphenylacetic acid (3,4-DHPA), which is excreted in urine and feces. The bioavailability of 3,4-Dihydroxy-5-methoxybenzoic acid is low due to its low solubility in water and high reactivity with proteins.

<p>Ethyl 4-amino-2-nitrobenzoate is a chemical intermediate that is used in the synthesis of other chemicals. It is also a versatile building block with many uses, such as in the production of research chemicals or as a reagent. It has CAS No. 84228-46-6 and can be purchased from various suppliers.</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>3-Chlorobenzoic acid is a compound that has been shown to have potent antibacterial activity against Pseudomonas aeruginosa and other bacteria. It has been shown to inhibit the ATP-binding cassette transporter, which is a protein that transports various molecules across cell membranes. 3-Chlorobenzoic acid also inhibits the growth of bacteria by lysing cells and interfering with DNA synthesis. This compound is an effective inhibitor of wild-type strains of E. coli, but not mutants resistant to 2,4-dichlorobenzoic acid. 3-Chlorobenzoic acid reacts with benzoate to form a crystal structure at room temperature and pressure. Further studies are needed to determine the coordination geometry and thermodynamic data for this reaction.</p>

3,5-Diisopropyl-4-hydroxybenzoic acid is a white, crystalline compound that can be found as a dimer. It is soluble in solvents such as chloroform and ethers but insoluble in water. 3,5-Diisopropyl-4-hydroxybenzoic acid is used in the production of polyesters, polymers, and resins. This compound has been used to produce propofol and decarboxylating monomers for organic solvents. 3,5-Diisopropyl-4-hydroxybenzoic acid reacts with chloride ion at high temperatures to form chlorine gas and hydrogen chloride. The melting point of this compound is 169 degrees Celsius.

<p>2-Ethoxy-4-nitrobenzoic acid is a nitrobenzoyl compound that is used as an anticoccidial drug. It has shown to be effective against coccidiosis in poultry. 2-Ethoxy-4-nitrobenzoic acid binds to the aminobenzoate moiety of the enzyme glutamic acid decarboxylase, thereby inhibiting its activity. This inhibits the production of lactic acid and leads to cell death by lack of energy. Amprolium is a coccidiostat that inhibits the synthesis of beta-alanine in cells, which leads to inhibition of protein synthesis and cell death.</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>2-Amino-5-methylbenzoic acid is an anthranilic acid derivative that has been shown to have potent antitumor activity. It inhibits the growth of cancer cells and is effective against light emission. 2-Amino-5-methylbenzoic acid blocks the production of porphyrins, which are necessary for the production of heme, a cofactor in many enzymes. The compound also inhibits serine protease, which is involved in tumor cell proliferation and metastasis.<br>2-Amino-5-methylbenzoic acid has been shown to inhibit the growth of human liver cancer cells in vitro. This compound can be synthesized by a Suzuki coupling reaction with phenylacetic acid and 3-(2'-aminoethyl)aminobenzene.</p>

<p>3,4-Dihydroxybenzoic acid ethyl ester (3,4-DHBA) is a phenolic compound that is used in the treatment of hepatic steatosis. 3,4-DHBA has been shown to be effective in inhibiting autophagy and may also be useful in the treatment of her2+ breast cancer. This drug has antioxidative properties and may also have a protective effect against myocardial infarct. 3,4-DHBA binds to iron ions and prevents their oxidation, thereby preventing oxidative stress. It has been shown to have low potency due to its short half-life in vivo. 3,4-DHBA can inhibit the mitochondrial membrane potential and lead to apoptosis of primary cells and tissue culture cells.</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.

4-Methoxybenzoic acid hydrazide is a copper complex that binds to the DNA of bacteria, inhibiting the production of proteins. It has been shown to have antimicrobial activity against gram-positive and gram-negative bacteria. 4-Methoxybenzoic acid hydrazide has also been shown to inhibit colorectal carcinoma cells in vitro and in vivo. This compound inhibits the growth of cells by binding to them and disrupting hydrogen bonds. 4-Methoxybenzoic acid hydrazide causes cell death by inhibiting protein synthesis.

<p>3,4-Dinitrobenzoic acid is a nitrobenzoic acid that has a hydrogen bond. 3,4-Dinitrobenzoic acid is activated by the loss of a proton and it reacts with amines to form diazonium salts. It can be found in plants and animals as an intermediate in the metabolism of tyrosine and tryptophan. 3,4-Dinitrobenzoic acid is used in analytical chemistry to detect the presence of amines. The functional groups on 3,4-dinitrobenzoic acid are carboxylic acid and nitro. Ribulose is an example of a molecule containing these functional groups.</p>

<p>3,4-Diaminobenzoic acid is a compound that is produced by the condensation of two molecules of hydrochloric acid. 3,4-Diaminobenzoic acid has been used as a reagent in the synthesis of coumarin derivatives. This chemical has been shown to be an effective proton scavenger in an optimum concentration. Benzimidazole compounds are also synthesized from 3,4-diaminobenzoic acid and have been shown to be effective against autoimmune diseases. 3,4-Diaminobenzoic acid can be used for the production of diazonium salts, which are used in the synthesis of anti-inflammatory drugs and other pharmaceuticals. The hydroxyl group on this molecule makes it chemically stable and kinetic data shows that it has high diphenolase activity.</p>

Methyl 3-bromo-2-fluorobenzoate (MBFB) is a versatile building block in chemical synthesis. MBFB can be used as a reagent or speciality chemical. It has been used as an intermediate for the synthesis of other compounds, such as methyl 5-bromo-2-fluorobenzoate and ethyl 5-bromo-2-fluorobenzoate. MBFB is also a useful scaffold for the synthesis of complex compounds with interesting functions, such as research chemicals.

<p>4,5-Dimethoxy-2-nitrobenzoic acid (DMNB) is a nitrophenol compound that is used as an intermediate in the synthesis of pesticides. DMNB inhibits the growth of bacteria through its ability to inhibit protein synthesis and DNA replication. The inhibition is due to DMNB’s ability to covalently bind to nucleophilic sites on enzymes that are essential for these processes. It has been shown that DMNB can be degraded by microorganisms, such as bacteria, fungi, and algae. The biodegradation process may be facilitated by its solubility in water and its low molecular weight.</p>

Ethyl 4-ethoxybenzoate is an antimicrobial agent that inhibits bacterial growth by interfering with the synthesis of DNA. It also has a genotoxic potential and can induce mutations in cells. Ethyl 4-ethoxybenzoate is used as an impurity in pharmaceutical drug production, such as solanum tuberosum extract, to prevent microbial contamination. It also has been shown to inhibit the growth of bacteria in cell cultures by binding to DNA and inhibiting DNA replication. Ethyl 4-ethoxybenzoate is used as a control agent for the detection of antibiotics in natural products, such as ethanol extracts from plants.

Dietary polyphenol

<p>3-Nitro-4-carbomethoxybenzoic acid is a thiophene that has been found to be an inhibitor of protein tyrosine phosphatase 1B (PTP1B). PTP1B is a key enzyme involved in the regulation of insulin secretion and blood sugar levels. 3-Nitro-4-carbomethoxybenzoic acid has been shown to inhibit PTP1B by mimicking the natural substrate of this enzyme, phosphotyrosine, and thereby preventing its dephosphorylation. It has also been shown to have anti-inflammatory properties.</p>

3-Chloro-5-hydroxybenzoic acid methyl ester is a fine chemical that can be used as a versatile building block and reaction component in the synthesis of complex compounds. It is soluble in organic solvents such as dichloromethane, chloroform, and acetone. 3-Chloro-5-hydroxybenzoic acid methyl ester has CAS No. 98406-04-3 and a molecular weight of 149. 2.

<p>3,4-Dimethoxybenzoic acid anhydride is a synthetic compound that can be used for the synthesis of other natural products. It has been shown to inhibit the demethylation of flavones and to activate the mitogen-activated protein kinase (MAPK) pathway in cells. 3,4-Dimethoxybenzoic acid anhydride has also been shown to have anti-inflammatory effects by inhibiting prostaglandin synthesis.</p>

<p>3-Methoxy-2,4,5-trifluorobenzoic acid (3MTBF) is a ligand that binds to the active site of bacterial dehydrogenases. It is used to inhibit the growth of bacteria in the environment and food products. 3MTBF inhibits the production of fluoroquinolones by methylating their chlorides with methoxy groups. This compound also has bifunctional properties, as it can act as both a methylating agent and an inhibitor of dehydrogenase enzymes. 3MTBF inhibits the production of cancer cells by inhibiting transcription and translation, preventing cell division and proliferation. 3MTBF is thermostable, meaning it does not break down in high temperatures or at pH extremes.</p>

2,5-Dimethylbenzoic acid is a compound that is found in urine samples. It is the product of the metabolism of 2,5-dihydroxybenzoic acid. 2,5-Dimethylbenzoic acid has a functional group which consists of a carboxylic acid group and two methyl groups. The acidic nature of this compound can be seen through its reaction with camphora, as well as its hydrolysis by hydrochloric acid. This compound also has protease activity when it comes into contact with human urine. 2,5-Dimethylbenzoic acid can be synthesized using solid-phase chemistry and chemical biology techniques. It has been shown to have a functional role in the production of proteins that are involved in cellular signaling pathways such as chemotaxis and apoptosis.

<p>3,5-Dimethyl-4-nitrobenzoic acid is a synthetic compound that has been used in the synthesis of other organic compounds. It is not currently used as a drug, but it has been shown to inhibit the growth of bacteria in vitro. The mechanism of action for this compound is unclear. 3,5-Dimethyl-4-nitrobenzoic acid has been shown to be active against the bacterium Typhimurium and may inhibit bacterial growth by being metabolised into nitrite or nitrate ions. This chemical can also be converted into a reactive intermediate that reacts with oxygen to form superoxide anion radicals, which are known to have antibacterial effects.</p>

<p>2-Chloro-4-trifluoromethylbenzoic acid is a chemical compound with the formula CHClFO. It can be obtained by deprotonation of 2,4,6-trichlorobenzoic acid with butyllithium and subsequent reaction with chlorotrifluoromethane. The product has two regioisomers, one in which the chlorine atom is attached to the para position on the benzene ring and the other in which it is attached to the ortho position. Substituents such as alkyl groups or lithium reagents can affect both reactivity and selectivity. The halogen substituent can also be replaced by other functional groups to make derivatives of this compound.</p>

4-Amino-5-chloro-2-methoxybenzoic acid is a compound that has been shown to be a potent 5-HT4 receptor agonist. It is used in the treatment of obesity and diabetes. The molecular structure of 4-Amino-5-chloro-2-methoxybenzoic acid consists of a carbonyl group and an amine group, which are bound to each other by a covalent bond. This molecule is found to bind to the 5HT4 receptor with high affinity, which leads to its efficacy as an antiobesity agent.

3,5-Dihydroxybenzoic acid is a phenolic compound that belongs to the class of aromatic compounds. It is an inhibitor of the enzyme 3-hydroxyphenylpyruvate dioxygenase and is used in the treatment of obesity. It has been shown to have a low potency for inhibiting this enzyme, although it does not inhibit other enzymes such as p-hydroxybenzoate hydroxylase. 3,5-Dihydroxybenzoic acid binds to human serum albumin through hydrogen bonding interactions and can inhibit the absorption of dietary phenols by binding to them. This compound also acts as a protocatechuic acid structural analog and has been shown to be hydrated in solution.

2-Ethynylbenzoic acid is an organic compound with a carboxylic acid functional group. It is an efficient method for the synthesis of amides from primary and secondary alcohols in the presence of a chloride donor, such as thionyl chloride. The reaction system is typically carried out in an organic solvent, such as dichloromethane or chloroform. The reaction mechanism proceeds by protonation of the alkene followed by nucleophilic attack by the amine on the carbonyl carbon atom. This step forms a tetrahedral intermediate that tautomerizes to give a furyl intermediate. The furyl intermediate then undergoes oxidative carbonylation to form 2-ethynylbenzaldehyde, which reacts with the amine to form 2-ethynylbenzoic acid. In this process, stereoselectivity can be achieved by using an acceptor that favors one enantiomer of 2-ethynylbenzaldehyde

Ethyl 4-N,N-diethylamino)benzoate is a molecule that contains a carbonyl group. In an exothermic reaction, the carbonyl group reacts with naphthalene in the presence of activated alkyl substituents to form a fluorescent product. The molecule has a constant and is monomeric. It has an aromatic hydrocarbon structure, which results in a red shift in the fluorescence emission spectrum. Ethyl 4-N,N-diethylamino)benzoate reacts with solvents such as water and alcohols to form solutes that are fluorescent.

<p>2-Benzoylbenzoic acid is an organic compound with the chemical formula C6H5CO2. It is a white solid that is soluble in water, ethanol, and ether. 2-Benzoylbenzoic acid is stable at room temperature, but decomposes when heated to above 200°C. This compound can be used as a catalyst for the synthesis of polymers.<br>2-Benzoylbenzoic acid is used as a raw material for the production of ferrocenecarboxylic acid and ethylene diamine. The activity index of 2-benzoylbenzoic acid was found to be high (0.7) when it was tested against Streptococcus mutans and Staphylococcus aureus.</p>

5-Fluoro-2-methylbenzoic acid is a synthetic compound that has antiviral potency against the influenza A virus. It is the active form of 5-fluoro-2-methylbenzoyl chloride, which is synthesized from a Grignard reagent and an asymmetric synthesis. 5-Fluoro-2-methylbenzoic acid has been shown to have anticancer properties in vitro, which may be due to its ability to inhibit cancer cell growth through interaction with chloride channels. This drug also inhibits the activity of dehydrogenases, which are enzymes that catalyze the oxidation of various substrates by reducing them.

2,3-Diaminobenzoic acid methyl ester is a redox potential catalyst that has been shown to have anticancer activity in vitro and in vivo. It is a 5-ht4 receptor agonist, which causes an increase in the intracellular concentration of cAMP. The anticancer effect of this compound may be due to its ability to inhibit the growth of cancer cells by blocking DNA synthesis and cell division. The biological properties of this drug are not well understood, but it has been shown to have antioxidant effects, as well as proton-reducing and electron-accepting properties. This compound has also been studied electrochemically.

Methyl 2-nitrobenzoate is a nitro compound that has been used to synthesize benzyl esters. It has been shown to react with protonation and acidic conditions. Methyl 2-nitrobenzoate is also used as an intermediate in the synthesis of methyl anthranilate, which is a component of artificial grape flavoring. The mechanism of the reaction is not fully understood, but it has been proposed that methyl 2-nitrobenzoate undergoes an intramolecular hydrogen bond with the benzoate group to form an intermediate compound called N-methyl-2-(phenylmethyl)benzamide. This intermediate then reacts with methylamine to form methyl anthranilate. The molecule can be detected by gas chromatography or liquid chromatography in organic solvents such as methanol or acetone.

4-Aminohippuric acid sodium (4AHA) is a drug that is used as a diagnostic tool for measuring renal plasma flow and renal function. The drug is administered intravenously and its optical properties are measured. 4AHA is filtered by the kidneys, which causes it to be excreted in urine. A sensor is placed on the patient's arm and measures the concentration of 4AHA in the blood flowing through the arm. This measurement can then be used to calculate renal plasma flow, which indirectly indicates kidney function. 4AHA can also be used to measure sodium levels in blood plasma, as it binds to sodium ions in solution. However, this application of 4AHA has been superseded by newer technologies such as ion-selective electrodes and magnetic resonance imaging, which offer improved accuracy at lower cost.

Inhibitor of redox-based NF-ΚB activation

<p>2,5-Dihydroxybenzoic acid is a natural compound that has been shown to inhibit the matrix metalloproteinase enzyme activity of α1-acid glycoprotein. The 2,5-dihydroxybenzoic acid structure is similar to p-hydroxybenzoic acid and gentisic acid. It is also an inhibitor of xanthine oxidase and caffeic acid oxidase. 2,5-Dihydroxybenzoic acid has a number of potential uses in analytical chemistry as it can be used to measure the concentrations of caffeic acids and other related compounds in biological samples.</p>

<p>3-Dimethylaminobenzoic acid is a carboxylate that can be found in plants and animals. It is a precursor to many biologically important molecules, including the amino acid tryptophan. 3-Dimethylaminobenzoic acid has been shown to have a redox potential of -0.38 V, which makes it an excellent candidate for use as an electron acceptor. This compound is also used as an intermediate in the synthesis of cholesterol esters and fatty acids, and has been shown to inhibit the growth of basophilic leukemia cells in mice. 3-Dimethylaminobenzoic acid has also been shown to have a cholesterol esterase activity on human liver cytosol, with an enzyme activity of 0.0015 U/mg protein at pH 7.5 and 37°C, and on human urine samples with an enzyme activity of 0.0027 U/mg protein at pH 6.0 and 37</p>

3,5-Diiodo-4-hydroxybenzoic acid (3,5 DIBA) is an aminotriazole that inhibits the growth of a wide range of bacteria. 3,5 DIBA inhibits the transport of catechol and 2,6-dichlorobenzoic acid into cells. This inhibition leads to decreased levels of catechol-O-methyltransferase activity and increased levels of lysine decarboxylase activity. The combination of these two reactions causes a decrease in lysine production. Lysine is important for cell division and protein synthesis in bacteria. 3,5 DIBA also inhibits root formation in plants and has been shown to inhibit the uptake of nutrients by plant roots. Also known as: Dibenzoylmethane; 1,2-Benzenediamine, 3-[(2,6-dichlorophenyl)imino]-, diiodide;

Methyl 4-acetamido-2-methoxybenzoate is a chemical compound that belongs to the group of heterocycles. It is a precursor to the imidazopyridine, imidazopyrazine and thiazolopyridine classes of drugs. The protonation of methyl 4-acetamido-2-methoxybenzoate has been shown experimentally to be an important factor in its biological activity, especially for its binding affinity for DNA. Methyl 4-acetamido-2-methoxybenzoate has been used as an inotropic agent and as an atypical antipsychotic drug.

3-Nitrobenzoic acid methyl ester is an organic compound that contains a hydroxyl group and a nitro group. It can be synthesized by the reaction of 3-nitrophenol and methanol in a solvent such as water or ethanol. The nitro group is important for the solvating power of this molecule, which has been shown to have approximations with other molecules. 3-Nitrobenzoic acid methyl ester is found in two different forms: the cis form and the trans form, which differ in the orientation of their nitro groups. The cis form is more stable than the trans form because it has a dipole moment. The vibrational frequencies are also higher for the cis form than for its trans counterpart. 3-Nitrobenzoic acid methyl ester has been shown to react with nintedanib, which is used to treat cancer, and inhibit kinetics. The kinetic data obtained from this study can

2-Fluoro-3-methylbenzoic acid is a high quality, versatile building block that has been shown to be an effective reagent for the synthesis of complex compounds. It is also a useful intermediate in the synthesis of fine chemicals and speciality chemicals. This compound can be used as a reaction component for many chemical reactions, such as the formation of new bonds and the removal of protecting groups. As a versatile building block, 2-fluoro-3-methylbenzoic acid is an important starting material for synthesizing a number of natural products, pharmaceuticals, and other organic compounds.

Ethopabate is a salt of ethopropazine and sodium carbonate. It is used in pharmaceutical preparations as an antiparasitic agent. The chemical composition of the salt is CHNO, with one hydrogen bond between the ethopropazine and sodium carbonate. Ethopabate has been shown to be active against amprolium-resistant coccidia in human serum, as well as being an analytical reagent for detecting monoclonal antibodies. This chemical can be used to prepare a polymeric matrix for use in fluorescence detection or for antimicrobial agents. Hydrochloric acid and UV light are used to synthesize this compound.

3-Methoxybenzoic acid is a compound that has two carboxyl groups, one on each of the two benzene rings. It is a white crystalline solid with a melting point of 86°C and a boiling point of 240°C at 1 mmHg. 3-Methoxybenzoic acid can be found in plants such as cranberries and strawberries. It also occurs naturally in animal fat, where it functions as an antioxidant and antimicrobial agent. 3-Methoxybenzoic acid has been shown to have synergistic effects when combined with protocatechuic acid in the treatment of carcinoma cells.

<p>n-Pentyl 4-hydroxybenzoate is a preservative that inhibits the growth of microorganisms. It is used in products such as cosmetics, pharmaceuticals, and food to prevent spoilage. The antimicrobial activity of n-pentyl 4-hydroxybenzoate has been shown to be due to p-hydroxybenzoic acid, which binds to bacterial cell walls. This binding prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division. n-Pentyl 4-hydroxybenzoate has also been shown to inhibit bacterial growth in vitro and in vivo in rats by interfering with protein synthesis in rat liver microsomes.</p>

<p>4-Chloro-3-hydroxybenzoic acid (4-CHB) is a reactive compound that can be used for the detection of bacteria. 4-CHB reacts with peroxyl radicals in solution to form a chlorobenzoic acid derivative, which emits light when excited by radiation. 4-CHB is also capable of dehalogenating chlorobenzene, and can be used as a bioluminescent probe for the detection of bacteria. The reactions are efficient at low concentrations and are detectable with an ultraviolet or visible spectrophotometer.</p>

2-Chloro-4-methoxybenzoic acid methyl ester is a reagent that can be used in the preparation of various compounds. It is also a versatile building block for the synthesis of complex compounds, such as pharmaceuticals and agrochemicals. This chemical is often used as an intermediate or building block in the preparation of pharmaceuticals and agrochemicals. 2-Chloro-4-methoxybenzoic acid methyl ester has been shown to be a useful scaffold for the synthesis of drugs with high quality and low cost.

<p>Flavoring agent; interacts with TPRV receptors and ASIC channels</p>

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2-Iodo-5-nitrobenzoic acid is a reactive molecule that reacts with terminal alkynes to form a fluorescent compound. It was immobilized on an electrode and used as a probe in voltammetry studies. 2-Iodo-5-nitrobenzoic acid is also used as a reagent in the synthesis of amides, which are important in many biochemical reactions. The use of this compound may be limited by the toxicity to cells, which can be increased through the presence of cisplatin or 3-aminobenzoic acid. The microenvironment around cancer cells may also alter the reactivity of 2-iodo-5-nitrobenzoic acid.

4-Hydroxy-3,5-dimethylbenzoic acid (4HDMBA) is an antimicrobial agent that inhibits bacterial cell growth by binding to the GyrA subunit of DNA gyrase. It is a potent inhibitor of the GyrA subunit, with activity against both mutant and wild type strains. 4HDMBA also has anticancer activity in vitro and in vivo studies have shown that it can inhibit the growth of cells from human cancer cell lines. 4HDMBA is synthesized by reacting amide with chloroacetyl chloride. The carboxylate group on 4HDMBA can be transformed into a hydroxyl group by reaction with sodium hydroxide. The chemical structure of 4HDMBA includes a hydroxy group, a chlorine atom, and a hydroxyl group.

Methyl 4-hydroxy-2-methylbenzoate is a chromophore. It has demonstrated antioxidant and anti-oxidative properties in a number of assays, including 3-ethylbenzothiazoline-6-sulfonic acid (EBT) assay, naphthalene oxidation assay, and electrocyclic test. Methyl 4-hydroxy-2-methylbenzoate has been shown to be bioactive with respect to steroids and lignans. This compound has also been used as a tyrosinase inhibitor in neocarzinostatin (NCS) synthesis. Methyl 4-hydroxy-2-methylbenzoate is found in the extract of the leaves of Ligustrum lucidum.

Methyl 2-methoxybenzoate is a synthetic chemical that is used in the treatment of wastewater. It inhibits the activity of enzymes such as fatty acid synthase, which are involved in the synthesis of long-chain fatty acids. Methyl 2-methoxybenzoate has been found to be an efficient method for the synthesis of prenyl compounds. This product is also an active methylene and hydrogen bond donor, and it can form products with carboxylic acid conjugates through acid catalysis. Methyl 2-methoxybenzoate has been used as a reagent for analytical chemistry, including gas chromatography and liquid chromatography.

2-Chloro-6-fluorobenzoic acid is an aromatic compound that is used as a solvent in the production of pharmaceuticals, plastics, and dyes. The 2-chloro-6-fluorobenzoic acid molecule has an electron rich ring structure that can undergo nucleophilic attack by a nucleophile such as hydrogen chloride or hydrochloric acid. It also has a high affinity for water molecules, which may be attributed to its aromatic hydrocarbon structure. This allows 2-chloro-6-fluorobenzoic acid to act as a good solvent for many organic compounds. This chemical is classified as a possible human carcinogen and is toxic to the liver cells.

Methyl 4-methoxybenzoate is a white, crystalline powder that is soluble in alcohol and ether. The chemical formula for methyl 4-methoxybenzoate is C8H10O4. It has a molecular weight of 196.19 g/mol and a melting point of 136°C. Methyl 4-methoxybenzoate has been used as an organic reagent, as well as a pharmaceutical intermediate and additive in food manufacturing. It also has biological properties such as being an anti-inflammatory agent and being able to inhibit the growth of infectious diseases like tuberculosis and malaria. Methyl 4-methoxybenzoate can be synthesized by reacting benzoic acid with methanol, phosphoric acid, or hydrochloric acid. This molecule can also be synthesized from p-hydroxybenzoic acid by electrophilic substitution with methyl iodide followed by hydrolysis using sodium hydroxide. The chemical

<p>4-Bromo-3,5-dimethoxybenzoic acid is a synthetic molecule that has been shown to have catalytic properties. It was generated by the reaction of resorcinol and dimethoxybenzoic acid in the presence of copper(II) acetate. This compound has also been shown to be bioinspired by its similarity to natural products such as 3,5-dihydroxybenzoic acid. 4-Bromo-3,5-dimethoxybenzoic acid has been used for the synthesis of bioactive molecules with cyclic structures. These advances are important for sustainable development and may help in the discovery of new natural products.</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>

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Methyl 4-bromo-2-methoxybenzoate is a drug molecule that belongs to the amide class. It is a synthetic reagent and can be used as a potential precursor in the synthesis of other drugs. Methyl 4-bromo-2-methoxybenzoate has been shown to react with carboxylic acids to form methyl esters, which are functional groups that contain a carboxyl group (COOH) and an alcohol group (OH). This reaction is called methoxylation. The transformation of methyl 4-bromo-2-methoxybenzoate into methyl esters increases the solubility of the compound and allows for it to be transported in water.

4,4'-Dibenzoic acid is a chemical compound that has been used as a precursor to other compounds. It is also used in the production of polycarbonates and epoxy resins. 4,4'-Dibenzoic acid has low energy, which means it can be transported more easily than high energy molecules. This property makes it an excellent candidate for use as an enhancement agent for organometallic catalysts such as biphenyl. The structure of 4,4'-dibenzoic acid consists of two benzene rings connected by an ethylene chain. This molecule has one hydrogen bond on each side of the molecule. The 4-hydroxyl group on the left side of the molecule is susceptible to oxidation and can act as an oxidation catalyst when exposed to heat or radiation.

<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>2-Amino-5-iodobenzoic acid (5-AIBA) is a chemical compound with a molecular weight of 152.14 g/mol. It belongs to the group of anthranilic compounds, and has antiinflammatory activity. 5-AIBA also inhibits cancer cell proliferation in vitro and in vivo by inhibiting the synthesis of DNA, RNA, and proteins. The reaction solution for the palladium-catalyzed coupling of 5-AIBA with 2-(N,N′-dimethylcarbamoyl)phenyl boronic acid was found to be stable at room temperature for 24 hours. The inhibitory activity of 5-AIBA against MCL1 protein was potent, as it inhibited MCL1 protein expression by 90%. Molecular modeling studies showed that 5-AIBA binds to the amide region on the ATP binding site in MCL1 protein (mcf7). Carbonyl groups are present on both sides of the am</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>2,5-Dimethyl-3-nitrobenzoic acid is a versatile building block that can be used in the synthesis of a wide range of compounds. It is also an important intermediate for the synthesis of pharmaceuticals and other speciality chemicals. 2,5-Dimethyl-3-nitrobenzoic acid has been shown to be useful in the preparation of high quality fine chemicals and research chemicals. This compound has been found to be an excellent reagent for various chemical reactions.</p>

3-Dimethylaminobenzoic acid is a bacterial enzyme that belongs to the group of p2 carboxylates. It is a non-specific esterase that has been shown to hydrolyze 3-ethylbenzthiazoline-6-sulfonic acid, which is an indicator of root formation. The enzyme activity of 3-dimethylaminobenzoic acid has been demonstrated in kinetic data and redox potential measurements. 3DMBB is found in plants and can be used for the determination of dry weight, as it can hydrolyze triticum aestivum urine samples or cholesterol esters. This enzyme also has catalase activity and can be used in the determination of catalase activity in biological fluids such as urine samples or blood serum.

4-Formyl-3-hydroxybenzoic acid (4FHB) is a member of the phenylacetic acid family. It has been shown to have potential as a substrate for creatine kinase and amines, as well as an inhibitor of the enzyme. 4FHB binds to the surface of silica particles in order to enhance Raman scattering in a solid-phase synthesis. The molecular weight of 4FHB is 148 g/mol, with optical properties that can be described by fluorescence spectroscopy. 4FHB has been shown to be homochiral and tetradentate, with a magnetic resonance spectrum that can be characterized by hydroxyl group and salicylaldehyde groups.

An intermediate in the phytocannabinoid biosynthetic pathway.

<p>2-Amino-4,5-dimethoxybenzoic acid is a potent antitumor agent that inhibits the growth of tumor cells. It has been shown to inhibit the production of epidermal growth factor (EGF) and plays a role in the inhibition of tumor cell proliferation in vitro. 2-Amino-4,5-dimethoxybenzoic acid has also been shown to have photochemical properties and can be activated by light. This compound can be used as an indicator for gravimetric analysis because it reacts with diazonium salts and produces a colored product. 2-Amino-4,5-dimethoxybenzoic acid is also reactive and may be used in Suzuki coupling reactions. This chemical compound is chemically related to other inhibitors such as mcf7 and suzuki coupling reactions.</p>

3-Amino-2,4,6-triiodobenzoic acid (3AIBA) is a chemical compound that is used as a contrast agent for medical imaging. It has been shown to be useful in the diagnosis of bladder cancer, and is used in the embolization of renal artery and ureteral calculi. 3AIBA functions by binding to the antigen binding sites on the tumor cells and allows visualization with X-rays. It has also been shown to be effective in reducing blood flow in tumors by blocking blood vessels with its cationic monomer. 3AIBA binds to the phosphate groups on DNA and causes crosslinking, which prevents DNA polymerase from binding with DNA. This inhibits DNA synthesis and cell division.

<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>

<p>3-Methoxy-4-methylbenzoic acid methyl ester is a potent inhibitor of the neurotoxic effects of β-amyloid peptide (Aβ) on cultured human neurons. 3-Methoxy-4-methylbenzoic acid methyl ester inhibits fibrillation in vitro and fluorescence assay, suggesting that it may be a promising therapeutic agent for Alzheimer's disease. The fluorescence assay is based on the inhibition of fluorescence by 3-methoxy-4-methylbenzoic acid methyl ester, which competes with Aβ for binding to an acceptor molecule. This inhibition can be used as a marker to measure the amount of Aβ present in vivo.</p>

<p>4-Toluic acid is a chemical compound with the molecular formula CH3C6H2O2. It is a white solid that is soluble in water and alcohol. 4-Toluic acid can be produced by oxidation of benzoate, which is a reaction catalyzed by light or by using a catalyst such as trifluoroacetic acid. The reaction mechanism begins with the formation of the intramolecular hydrogen and subsequent oxidation to form an organic radical. This organic radical then reacts with oxygen to produce 4-toluic acid. 4-Toluic acid has been shown to have biochemical properties such as enzyme inhibition, DNA cleavage, and protein denaturation. The coordination geometry for this molecule is octahedral, and its redox potentials are -0.27 V (in acidic solution) and -1.06 V (in alkaline solution).</p>

<p>Please enquire for more information about 3-Chloro-5-hydroxybenzoic acid ethyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Component in some dental cements</p>

3,5,6-Trichlorosalicylic acid binds to the active site of bacterial 5-nitrosalicylic acid reductase and inhibits its activity. It is an inhibitor of proton-translocating ATPases. 3,5,6-Trichlorosalicylic acid has been shown to be effective against a variety of bacteria at low concentrations. 3,5,6-Trichlorosalicylic acid has also been shown to inhibit some physiological activities such as the light emission and chemiluminescent reaction of luciferin in fireflies. This chemical reacts with chloride ions to produce light.

<p>Ethyl 2-nitrobenzoate is a cyclic organic compound that contains a nitro group, which is an organic radical with the formula -NO2. It belongs to the class of amides and has two carbonyl groups. The molecule consists of a bicyclic heterocycle consisting of one ring with five carbon atoms and one ring with six carbon atoms. Ethyl 2-nitrobenzoate can be used in the treatment of muscle diseases, metabolic disorders, growth factor deficiencies, autoimmune diseases, and neural system disorders due to its ability to act as an antihypertensive agent and as an inhibitor of angiotensin converting enzyme (ACE). This molecule's hydroxyl group can also react with epidermal growth factor (EGF) to form N-hydroxyethyl EGF (NHE). This product has been shown to have antiviral properties against HIV-1 protease inhibitors by interfering with viral protein synthesis.</p>

<p>Ethyl 3-aminobenzoate is a chemical that is used as an anesthetic. It is administered intravenously and has been shown to have effects on the cardiovascular system, such as lowering blood pressure, decreasing heart rate and increasing the time it takes for the heart to recover after a contraction. Ethyl 3-aminobenzoate also affects the central nervous system by causing anesthesia and changes in brain function. Its effects are reversible with administration of naloxone or flumazenil.</p>

2,4-Difluoro-3-hydroxybenzoic acid methyl ester is a fine chemical that is used as a versatile building block for research chemicals and other complex compounds. It can be used as a reaction component in the synthesis of new chemical entities or as a reagent for organic chemistry reactions. 2,4-Difluoro-3-hydroxybenzoic acid methyl ester has CAS No. 194804-80-3 and is available in high quality.

<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>2-Amino-3-methylbenzoic acid is an organic compound with the formula H2CCH(NH2)(COOH). It is a white solid that is soluble in water. The molecule has a planar geometry, and the copper ion is coordinated by four oxygen atoms and three nitrogen atoms. This coordination geometry can be seen in the crystal structure of the molecule. 2-Amino-3-methylbenzoic acid has been shown to have antifungal activity against Aspergillus niger. It also inhibits 5-nitrosalicyclic acid and sodium carbonate, which are involved in the synthesis of nicotinamide adenine dinucleotide phosphate (NADPH) and ATP respectively. 2-Amino-3-methylbenzoic acid has also been shown to inhibit ryanodine receptor channels, which are important for calcium release from endoplasmic reticulum.</p>

N-Phenylanthranilic acid is a nonsteroidal anti-inflammatory drug that inhibits the activity of cyclooxygenase-1 and cyclooxygenase-2. It has been shown to be effective against congestive heart failure in animal models. N-Phenylanthranilic acid also possesses potent anti-inflammatory activities that are mediated by inhibiting the production of prostaglandins. The compound binds to DNA and blocks the binding of transcription factors, leading to cell death. N-Phenylanthranilic acid has been shown to inhibit proliferation in human erythrocytes and k562 cells, as well as apoptosis pathway in these cells.