Benzenes

<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>2,4-Dimethoxybenzaldehyde is a synthetic compound that has been shown to have activity against pancreatic lipase. It has been suggested as a potential drug for the treatment of metabolic disorders such as obesity or diabetes. 2,4-Dimethoxybenzaldehyde can be synthesized by reacting ethyl diazoacetate with an aldehyde in the presence of ammonium acetate. This chemical can also be used to produce ethyl esters and compounds belonging to the group of phlorotannins. 2,4-Dimethoxybenzaldehyde has been shown to have antioxidative activity and inhibitory effects on pancreatic lipase.</p>

<p>4-Ethoxy-3-hydroxybenzaldehyde (4EHB) is a thioacetal that has been shown to be an effective precursor for the synthesis of many other molecules, such as combretastatin a-4. It is prepared by reaction of ethylmagnesium bromide and acetone. 4EHB has been shown to have antifungal properties in vitro, and can be used in the treatment of cancer cells. This compound is volatile and can be easily detected with headspace techniques. The functional group of this molecule is an alcohol group, which is found on the ring structure. Spectroscopic analysis shows that it has a carbonyl group with an OH group attached to it.</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>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>

<p>Ethyl 2,4-dihydroxy-6-methylbenzoate is a phenolic acid that is found in lichens. It has been shown to have anti-cancer and anti-inflammatory properties. The hydrogen bonds of ethyl 2,4-dihydroxy-6-methylbenzoate are the result of an intramolecular hydrogen bonding between the benzoic acid group and the hydroxymethyl group. This compound can also be found in matrix effect health care products as well as wastewater treatment plants. Ethyl 2,4-dihydroxy-6-methylbenzoate has also been shown to inhibit enzymes such as uv absorption and phenolic acids.</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>4-Dimethylamino-2-methoxybenzaldehyde is a chemical used as a research reagent and intermediate. It can be used to synthesize other compounds, such as pharmaceuticals, pesticides, and agrochemicals. It is also useful in the production of various dyes, pigments, and fragrances, representing effective staining under anaerobic conditions. CAS No. 84562-48-1</p>

<p>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</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>

<p>5-Bromo-2-methoxybenzaldehyde is a benzodiazepine receptor ligand that has been shown to have antiviral, antibacterial and anticancer properties. 5-Bromo-2-methoxybenzaldehyde is an inhibitor of the enzyme benzyl alcohol dehydrogenase (BAHD). BAHD plays an important role in the production of reactive oxygen species (ROS) by converting benzoic acid to benzoate, which is then converted to ROS. The inhibitory concentration values for 5-bromo-2-methoxybenzaldehyde are not yet known.</p>

<p>2,4-Dimethoxy-5-methylbenzaldehyde is an aryl aldehyde that can be synthesized from 2,4-dimethoxyphenol and methyl benzoate. It can also be produced by condensation of benzaldehyde with chloroform in the presence of zinc chloride. This compound is used in the production of various pharmaceuticals, including antihistamines, antidepressants, and antipsychotics.</p>

<p>6-Bromoveratraldehyde (6BrA) is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and has been used as a model study for biphenyl and naphthalene. 6BrA induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell.</p>

<p>3-Methoxybenzaldehyde is a chemical compound that is used as an intermediate in the synthesis of organic compounds. This compound has shown to be a potent inhibitor of several enzymes, including diamine tetraacetic acid (DAT)-dependent aminotransferase, trimethyl amine N-oxide reductase, and hydrochloric acid hydrolases. 3-Methoxybenzaldehyde also inhibits the growth of hepg2 cells and induces apoptosis. The chemical structure of this compound contains a boron nitride group that can form hydrogen bonds with other molecules and fatty acids that can act as a substrate for oxidation reactions.</p>

<p>3-Iodo-4-methylbenzoic acid is a synthetic growth factor that is used in the production of monoclonal antibodies. It is synthesized by reacting 3-iodo-4-methylbenzoic acid with trifluoroacetic acid, then purified by dispersive solid-phase extraction. The synthesis of 3-Iodo-4-methylbenzoic acid requires a labeling agent to be added to the reaction mixture for detection purposes. The labeled compound can be detected using assays such as radioimmunoassay or ELISA. In order to synthesize 3-Iodo-4-methylbenzoic acid, methyl esterification of 3-(2′,2′,2′,-trichloroethoxy)phenylacetic acid is required. This process involves an organic solvent and bromine as a catalyst. This compound has been shown to inhibit the BCR/ABL tyrosine kinase receptor</p>

<p>2,4,6-Trihydroxybenzaldehyde is a polymerase chain inhibitor that blocks the synthesis of DNA and RNA. It has been shown to have significant cytotoxicity in vitro and has been used as an antimicrobial agent to inhibit the growth of bacteria. 2,4,6-Trihydroxybenzaldehyde also inhibits tetracycline resistance in Mycobacterium tuberculosis (Mtb) by inhibiting the production of proteins vital for bacterial cell division. This compound is structurally related to naturally occurring compounds such as anthocyanins and it has been shown to have inhibitory properties on mitochondrial membrane potential, which may be due to its ability to inhibit protein synthesis and induce apoptosis. The analytical methods used for this compound are thin layer chromatography and high performance liquid chromatography.</p>

<p>3-Methyl-4-nitrobenzonitrile is a fluorescing aromatic amine that is synthesized by aliphatic amines. It has been shown to inhibit the growth of cells in culture, which may be due to its ability to bind with and inhibit the insulin-like growth factor receptor-1 (IGF-1R). 3-Methyl-4-nitrobenzonitrile has also been shown to bind with cytochrome P450 enzymes, where it can be oxidized or reduced. The conformation of 3-methyl-4 nitrobenzonitrile is dependent on the solvent molecules present.</p>

<p>Vegetable, nutty and floral flavour/fragrance</p>

<p>3-Hydroxy-4-iodobenzaldehyde is a fluorophore that is used in the synthesis of amide compounds, as well as in the production of other synthetic molecules. 3-Hydroxy-4-iodobenzaldehyde has been shown to have pharmacokinetic properties that are similar to those of fluorescein, and can be used to study the distribution and metabolism of this compound. This compound also has an oxidation potential that is higher than that of fluorescein, which makes it more useful for studying drug metabolism. The labile nature of 3-hydroxy-4-iodobenzaldehyde means it will not remain intact for long periods of time.</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>3-Hydroxybenzylamine hydrochloride (3HBH) is a chemical compound that has been used as a reagent and in the synthesis of other compounds. It is also known to be a useful scaffold for complex compounds, and can be used as a building block for the synthesis of fine chemicals. 3HBH has been found to have many applications in research, such as being an intermediate for pharmaceuticals, pesticides, dyes, and agrochemicals. 3HBH is also useful in organic syntheses where it has been found to react with nitriles and amides to form esters and amides respectively.</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>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>

<p>2,4,6-Tribromo-3-hydroxybenzaldehyde (2,4,6-TBHB) is an aldehyde that is synthesized from the reaction of 2,4,6-trichlorobenzaldehyde and bromine. It has been shown to be cytotoxic in tumour cell lines in vitro. This compound binds to DNA by covalent binding and inhibits the synthesis of proteins. 2,4,6-TBHB also inhibits cellular uptake of halides such as chloride and bromide ions. This aldehyde has been shown to induce cell death in human lung cancer cells in a concentration dependent manner.</p>

<p>3-Hydroxy-5-nitrobenzaldehyde is a solvent that has been used as a probe to measure chloride concentration in multimedia. It can be used as a sensor and an algorithm to detect the colorimetric change of 3-hydroxy-5-nitrobenzaldehyde in the presence of chloride ions. This probe is also used in colorimetric tests for linker, nonpolar, and surfactant compounds. The 3-hydroxy-5-nitrobenzaldehyde oxime can be cleaved by UV light to produce an unstable nitronium ion that reacts with metal ions such as copper(II) or silver(I) to form an insoluble precipitate.</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>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>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>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-Amino-4-methoxy-benzoic acid methyl ester is a high quality, versatile building block for the synthesis of complex compounds. It is an intermediate in the synthesis of a number of biologically active compounds and has been used as a reagent for the determination of amino acids. 2-Amino-4-methoxy-benzoic acid methyl ester is soluble in water and polar organic solvents.</p>

<p>5-Bromo-2-nitrobenzoic acid is a chemical compound that belongs to the group of bromonitrobenzenes. It is an important intermediate in organic chemistry and has been used as a reagent for the synthesis of various heterocyclic compounds. 5-Bromo-2-nitrobenzoic acid can be used as a building block for pharmaceuticals, agrochemicals, dyes, and other chemicals. This versatile chemical has been widely used in research and development as a reaction component for synthesizing pharmaceuticals or speciality chemicals or as a building block to produce useful scaffolds.</p>

<p>3-Hydroxybenzaldehyde (3HBA) is an organic molecule that belongs to the group of substituted benzaldehydes. It has been shown to induce muscle cell proliferation in vitro and in vivo, as well as increased levels of activated caspase-3 in vitro. 3HBA also has a high resistance to hydrochloric acid, hydrogen bond, and chemical structures. It also shows properties of intramolecular hydrogen bonding and aldehyde groups. 3HBA has been shown to be active against malonic acid-induced pulmonary edema in rats, which may be due to its ability to inhibit the release of erythrocytes from the bone marrow into the circulation.</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>2-Methyl-3-nitrobenzoic acid is a diketone that is used as a synthetic building block for the synthesis of fatty acid esters. This compound is also used to normalize butyric acid levels in blood, and has been shown to inhibit the formation of coumarin derivatives from nitrosalicylic acid. 2-Methyl-3-nitrobenzoic acid is an organic molecule with a molecular weight of 128.17 g/mol, and has four functional groups: two methyl groups, one carboxyl group, and one phenyl group. The compound reacts with a solution containing nitrite ions in an acidic environment to form nitrous acid (HONO) and 2-methylene-3-nitrobenzaldehyde (2MNB). 2MNB is soluble in water and has a solubility data of 0.0012 g/100 mL at 25 degrees Celsius.</p>

<p>2-Hydroxy-6-methoxybenzaldehyde is a molecule that can form hydrogen bonds with other molecules. FT-IR spectroscopy has shown that this compound has a copper complex and an acidic proton, which may be due to intramolecular hydrogen bonding interactions. The compound also has been shown to have potent inhibitory activity against cellular growth and cancer cells in vitro. 2-Hydroxy-6-methoxybenzaldehyde is a metal chelator and can therefore bind to metals such as iron and copper. It is genotoxic, which means it damages DNA by causing DNA strand breaks or crosslinks, leading to cell death. This chemical may also cause genetic mutations through the formation of tautomers that make DNA replication difficult. Gel chromatography shows that 2HMB has a low molecular weight (MW) and high solubility.</p>

<p>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.</p>

<p>2-Nitrobenzoic acid is an organic compound that is used as a reagent in the preparation of aldehydes, esters, and amides. It has been shown to be a potent inhibitor of the MCL-1 protein. This protein is an important regulator of mitochondrial permeability transition pore (MPTP) opening and apoptosis induction. The inhibition of the MPTP by 2-nitrobenzoic acid may be due to its ability to react with nitric oxide (NO) to form peroxynitrite, which reacts with MPTP proteins in the mitochondria. The use of 2-nitrobenzoic acid has been found to be effective in treating infectious diseases such as HIV, as well as autoimmune diseases such as psoriasis.</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>2,5-Difluoro-3-methylbenzoic acid methyl ester is a high quality, complex compound that can be used as a versatile building block in synthesis. It acts as a reagent and can be used as a research chemical. 2,5-Difluoro-3-methylbenzoic acid methyl ester is an intermediate in the production of other chemicals and can also be used as a reaction component or useful scaffold.</p>

<p>3-Iodobenzaldehyde is an atypical, isomeric, low energy, functional group. It has a fluorine atom in the 3-position and three different types of functional groups: alcohol, aldehyde and carboxylic acid. This compound has been studied for its ability to bind to receptors. 3-Iodobenzaldehyde can be synthesized by reacting benzalchohde with iodine and hydrochloric acid. The technique used to produce this compound is called Grignard reaction. 3-Iodobenzaldehyde can also be prepared by heating the corresponding nitrobenzene with sodium iodide in dry ether or under refluxing conditions. This compound has a low boiling point and melts at about 170 degrees Celsius. The frequency of this molecule ranges from 98 to 102 megahertz</p>

<p>3',4'-Dihydroxyphenylacetone (DOPA) is a metabolite of dopamine that is produced in the brain and kidneys. DOPA has been shown to have pharmacological properties, but its function as an endogenous neurotransmitter has not been confirmed. DOPA is also a precursor for the synthesis of melanin, which is found in skin cells. The detection of DOPA in urine samples can be used to diagnose Parkinson's disease or other conditions characterized by low levels of dopamine. The enzyme glutamate dehydrogenase converts DOPA into 3-methoxytyramine, which can be detected in urine samples using chromatographic methods. 3',4'-Dihydroxyphenylacetone may be measured in the blood plasma of patients with bacterial infections and urinary tract infections. A detectable concentration of this metabolite could indicate that the body is making use of an alternate pathway for synthesizing amines.</p>

<p>5-Carboxyvanillic acid is a chemical compound that belongs to the class of organic compounds known as carboxylic acids. It is also called o-vanillin, and it has a molecular weight of 116.19 g/mol. 5-Carboxyvanillic acid is one of the main ingredients in natural vanilla flavour. The hydroxyl group on the 5th carbon atom of this molecule reacts with a proton, which results in an addition reaction mechanism. The reaction proceeds through two steps: first, protonation occurs at the 5th carbon atom; second, deprotonation occurs at the 4th carbon atom. This chemical compound can be found as a white crystalline solid and as a volatile oil.</p>

<p>2-Amino-5-nitrobenzoic acid is a plant metabolite that contains a nitro group. It has been found to be an effective inhibitor of glutamate dehydrogenase, one of the enzymes involved in the metabolism of amino acids. 2-Amino-5-nitrobenzoic acid has also been shown to have no effect on other enzyme activities such as amines and nitrosamines. This natural product has been shown to be useful as a model system for understanding how hydrochloric acid interacts with plants, by inhibiting their growth.</p>

<p>4-Hydroxybenzoic acid sodium salt (4HBA) is a drug that is used in the treatment of bowel disease. It is an antimicrobial agent that has been shown to have activity against Gram-positive and Gram-negative bacteria, including Pseudomonas aeruginosa. 4HBA has also been shown to be effective in the treatment of ulcerative colitis and Crohn's disease by reducing the production of inflammatory cytokines. The mechanism of action for 4HBA is not fully understood, but it may be due to its ability to interfere with protein synthesis in bacteria, as well as inhibit antibody responses in humans. The structural biology studies on this compound have revealed that the α subunit can bind to the β subunit, which could affect its activity.</p>

<p>3-Methylphenylacetone is a dioxane with functional groups, which can be synthesized by coupling of acetoacetate and nitrobenzene. 3-Methylphenylacetone is a versatile precursor for the synthesis of various esters, such as phenylethyl acetate. This compound can also be deacylated to form 3-methylphenol, which is used in the synthesis of nitrophenols. In addition, 3-methylphenylacetone can be used in the production of acetophenones, ketones, and other aromatic compounds by using catalysts such as iodine or phosphoric acid. Nitro groups on 3-methylphenylacetone react with chloro-, bromo-, or methoxy-substituted substrates to form nitrosated derivatives. The tert-butyl group is eliminated spontaneously to form an amine.</p>

<p>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.<br> <br>The molecule can be detected by gas chromatography or liquid chromatography in organic solvents such as methanol or acetone.</p>

<p>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.</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>2-Fluoro-4-isopropyloxybenzoic acid is a fluorescent reagent with a high quality and purity. It is a complex compound that can be used as an intermediate in the synthesis of fine chemicals, pharmaceuticals, pesticides, herbicides, and other useful compounds. 2-Fluoro-4-isopropyloxybenzoic acid is also used as a starting material for the synthesis of speciality chemicals such as reaction components and versatile building blocks. It is soluble in organic solvents and has been shown to react with various functional groups.</p>

<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>

<p>4-Amino-3,5-diiodobenzoic acid is a conjugate of the amino acid histidine with two iodine atoms. It is used as a radiopaque contrast agent for X-ray imaging and has been shown to be useful in distinguishing between normal tissue and cancerous lesions. The molecule can be modified to contain various functional groups that allow it to bind to other molecules such as proteins or DNA, which can alter its properties. 4-Amino-3,5-diiodobenzoic acid is also known as diaminobenzene diiodide and is soluble in water.</p>

<p>2-Hydroxy-4-nitrobenzaldehyde is a molecule that reacts with kinase receptors in cancer cells and causes oxidative carbonylation. It has been shown to react with chloride, salicylaldehyde and dobutamine to form a fluorescent compound, which can be used as a probe for fluorescence studies. The fluorescence properties of 2-hydroxy-4-nitrobenzaldehyde have also been exploited for the development of pyrazoles as potential anti-cancer agents.</p>

<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>

<p>The compound 4-Bromo-3,5-dihydroxybenzoic acid methyl ester is an ether that is a natural product. It has been shown to have diastereoselective coupling with phenolic groups and unsymmetrically with lactones. This compound also undergoes epoxidation and farnesylation reactions. The intramolecular chain of the ether is methylated by formylation and reductive elimination.</p>

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

<p>2,4,6-Trihydroxybenzoic acid methyl ester is a synthetic compound that has been used in animal studies to investigate the inflammatory effects of substances. It has been shown to have anti-inflammatory properties in vitro and in vivo. Furthermore, 2,4,6-Trihydroxybenzoic acid methyl ester has been shown to inhibit the production of tumour necrosis factor-α (TNF-α) and other cytokines. This drug also has anti-fungal activity against Candida albicans and Aspergillus fumigatus. 2,4,6-Trihydroxybenzoic acid methyl ester is biodegradable.</p>

<p>4-Acetamidobenzaldehyde is an organic compound that has been shown to exhibit inhibitory effects on influenza virus replication in cell culture. 4-Acetamidobenzaldehyde is a dihedral molecule with a p2 group and can be synthesized from benzaldehyde and acetamide. It has also been shown to have potential use in the treatment of tuberculosis. The biological properties of 4-acetamidobenzaldehyde are not well understood, but it is thought that uptake may occur through the imine nitrogen. This molecule has been detected in tissue samples such as lung, liver, and kidney.</p>

<p>3,5-Difluoro-4-hydroxybenzaldehyde is a biochemical that belongs to the group of anticancer agents. It is activated by hydroxyl radicals and inhibits cancer cells. 3,5-Difluoro-4-hydroxybenzaldehyde inhibits protein synthesis in the cell by binding to messenger RNA and preventing its translation into protein. This compound also has inhibitory properties against DNA polymerase, which prevents DNA replication and transcription. 3,5-Difluoro-4-hydroxybenzaldehyde can be used as a template for oligodeoxynucleotides (ODN) to enhance photochemical properties.</p>

<p>4-Benzyloxy-3-methoxybenzaldehyde is a deuterium isotope analog of the natural compound benzaldehyde. This molecule has been shown to inhibit the growth of cancer cells in tissue culture by binding to DNA. The molecular mechanism of this inhibition is believed to involve an enzymatic process that results in the substitution of chloride for chlorine, thereby inhibiting DNA synthesis and preventing cell division. 4-Benzyloxy-3-methoxybenzaldehyde also inhibits the production of growth factors and thus has anticancer activity.</p>

<p>4-Iodobenzoic acid is a chiral compound that can be used as a nutrient solution in the laboratory. It has been shown to be effective at removing p-hydroxybenzoic acid and 4-dimethylaminobenzoic acid from wastewater. The reaction mechanism of 4-iodobenzoic acid involves intramolecular hydrogen transfer from the hydroxyl group on the benzoic side chain to the iodine atom, which forms an intermediate that reacts with a second molecule of benzoic acid. This reaction mechanism is similar to that found in caproic acid, except for the substitution of hydrogen with iodine. The addition of sodium hypochlorite or potassium permanganate can lead to the oxidation of 4-iodobenzoic acid and its eventual decomposition into carbon dioxide and water.</p>

<p>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.<br>Methyl 4-hydroxy-2-methylbenzoate is found in the extract of the leaves of Ligustrum lucidum.</p>

<p>3-Bromo-2,6-dimethoxybenzoic acid is a synthetic chemical used to introduce insulators into the DNA molecule. It is also used as a treatment method for introducing branched-chain scripts into the DNA molecule. 3-Bromo-2,6-dimethoxybenzoic acid has been shown to counteract synthetic techniques, such as transistors, and can be used in plant physiology research.</p>

<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>

<p>2-Chloro-3-methylbenzylamine HCl is a fine chemical that is a versatile building block for synthesis of pharmaceuticals and research chemicals. It is also a useful intermediate in the production of other compounds, such as speciality chemicals, complex compounds, and reaction components. 2-Chloro-3-methylbenzylamine HCl has many potential applications in both academia and industry because it is a high quality reagent with many uses.</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-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>2-Amino-6-chlorobenzoic acid is a reactive compound that can be used as an antimicrobial agent. It binds to the active site of enzymes and inhibits their function, thereby preventing bacterial growth. 2-Amino-6-chlorobenzoic acid also has acidic properties, which may be due to its ability to hydrolyze esters by acting as a dehydrating agent. This chemical is thermodynamically stable and can be synthesized from malonic acid or other compounds. The chemical reactions of 2-amino-6-chlorobenzoic acid can be followed by NMR spectroscopy, which provides the structural information about the molecule. The reaction mechanism for 2-amino-6-chlorobenzoic acid is similar to that of amides.</p>

<p>2,3,4-Trimethoxy-6-methylbenzaldehyde is a synthetic coumarin with antibacterial activity. It is synthesized by the condensation of 3-hydroxyacetophenone and benzaldehyde. 2,3,4-Trimethoxy-6-methylbenzaldehyde has been shown to have antibacterial activity against both Gram-positive and Gram-negative bacteria. This molecule has also been shown to inhibit the growth of Gram negative bacteria in the presence of hydrogen peroxide. The crystal structure of this molecule was determined by XRD analysis and shows that it contains a dihedral angle of about 155°.</p>

<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>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.</p>

<p>4-Chloro-2-fluorophenyl)acetic acid ethyl ester is a fine chemical that can be used as a scaffold for building more complex molecules, or it can be used as a versatile building block in the synthesis of research chemicals. It is also an intermediate in many reactions and can be used as a speciality chemical. 4-Chloro-2-fluorophenyl)acetic acid ethyl ester has been shown to have high quality and it is useful for research on complex compounds. It can also be used as a reagent in organic synthesis.</p>

<p>Please enquire for more information about 3,4-Dihydroxybenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,4-Dihydroxybenzaldehyde (2,4DBA) is a copper complex that has been shown to have biological properties. This compound has been studied in biological studies and is classified as group p2 on the periodic table. It is a redox potential of -0.95 V and can undergo intramolecular hydrogen bonding with itself or with other molecules to form hydrogen bonds. Hydroxyl groups are found on 2,4DBA and can coordinate with the nitrogen atoms found on penicillin-binding proteins or acetylcholinesterase inhibition. The coordination geometry of 2,4DBA is tetrahedral and its methyl ethyl group is also found on this molecule.</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>4-Ethylbenzonitrile is a chemical that is found in human lung. It is a terminal alkene, which undergoes aerobic photooxidation to form reactive oxygen species such as superoxide radical anion and hydrogen peroxide. 4-Ethylbenzonitrile is also converted to triazine, which has been shown to have tumorigenic properties in the lungs of rats and mice. The functional groups on 4-ethylbenzonitrile are amines, hydroxyls, carbonyls, and nitriles. This compound has an inhibitory effect on lung fibroblasts due to its ability to interfere with the function of β-unsaturated ketones. 4-Ethylbenzonitrile's basic structure contains three carbon atoms, two double bonds, and one triple bond.</p>

<p>Ethyl 4-iodobenzoate is an amide that reacts with a variety of substances, including retinoic acid and pemetrexed. It is a reactive substance that can be used in the synthesis of other substances such as iron oxides and transfer mechanism. Ethyl 4-iodobenzoate is also used for the preparation of picolinic acid and crystalline structure. Radical coupling reactions are most common and involve halides, phenyl groups, and aryl halides. The reaction temperature ranges from room temperature to 100 ˚C, while the reaction mechanism varies depending on the type of coupling reaction.</p>

<p>4-Iodobenzaldehyde is a chemical compound with the molecular formula C6H5IO. It is an aromatic compound that can be used in cancer therapy. 4-Iodobenzaldehyde reacts with trifluoroacetic acid to form an intramolecular hydrogen, which is detected using a low-energy monomer and high detection sensitivity. 4-Iodobenzaldehyde has two phenyl substituents and a serine protease functional group, which are required for its interaction with other molecules. The presence of these functional groups allows analytical methods to be used to identify 4-iodobenzaldehyde in various samples. Using analytical methods, it can be determined that 4-iodobenzaldehyde interacts with an acceptor molecule at the reaction vessel thermally or by irradiation.</p>

<p>2-Methoxybenzoic acid is a nonsteroidal anti-inflammatory drug that belongs to the group of acetate extract. This compound has been shown to inhibit the production of prostaglandin E2 by inhibiting cyclooxygenase activity. 2-Methoxybenzoic acid also acts as an antagonist at serotonin 5HT1A receptors, which are involved in the regulation of mood and cognition. It is a competitive inhibitor of p-hydroxybenzoic acid, natural compounds, and protocatechuic acid with hydrogen bond interactions. 2-Methoxybenzoic acid also binds to tissue culture cells and inhibits cell growth through receptor binding.</p>

<p>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>

<p>3,5-Dibromo-4-methoxybenzonitrile (DBMB) is a pentane that can be synthesized in the laboratory. DBMB is used as a weed control agent to kill weeds and grasses in neoprene rubber products and other materials. The chemical reacts with nitro groups on the surface of the material, producing an unstable intermediate that decomposes into pentane and nitric acid. 3,5-Dibromo-4-methoxybenzonitrile has been shown to have low toxicity to mammals at high doses.<br>The compound may also be used as a chemical intermediate for the synthesis of other compounds or drugs. Nitro groups may be reduced by reductants such as sodium borohydride or lithium aluminium hydride to produce analdehyde derivatives.</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>

<p>4-Fluoro-3-hydroxybenzoic acid is a colorless solid that can be produced through the sulfonation of 4-fluorophenol with sulfuric acid. This process usually takes place in two steps: first, the phenol is refluxed with sulfur trioxide and then aqueous potassium hydroxide is added to the mixture. The reaction produces a sulfite salt, which is then treated with sodium sulfite to produce the desired acid. 4-Fluoro-3-hydroxybenzoic acid can also be synthesized by adding sulfur dioxide to an aqueous solution of 3% hydrogen peroxide and adding potassium hydroxide dropwise until effervescence ceases. This method produces an insoluble precipitate, which is filtered out and washed with water. The product can then be purified by recrystallization from hot water or by washing with ether.</p>