10-540008 - 3-benzoylbenzoic-acid | 5

<p>3-Benzoylbenzoic acid has been used in light-induced reactions on benzophenone-terminated boron-doped diamond (BDD) surfaces and preparation of benzophenone flavonol derivative. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation</p>

3-Benzoylbenzoic Acid

<p>Benzophenone-3-carboxylic acid is a chemical compound that is used in the production of polymeric photoinitiators. It has been shown to have an absorption maximum at 350 nm and to convert to benzophenone-3-carboxylic acid upon exposure to ultraviolet light. Benzophenone-3-carboxylic acid can also be reduced by trifluoroacetic acid or carbonyl compounds such as hippuric acid, forming benzophenone-3 and fatty acids. The use of benzophenone-3-carboxylic acid in polymeric photoinitiators has been shown to reduce the emission of volatile organic compounds (VOCs) from coatings.</p>

<p>Applications 2-(3-Amino-4-chlorobenzoyl)benzoic Acid is a useful synthetic intermediate. It is used to prepare protein kinase C phosphorylates synthetic fluorescent reporter.<br>References Chen, C., et al.: J. Am. Chem. Soc., 124, 3840 (2002)<br></p>

<p>3-Hydroxybenzophenone is a benzoate that can be found in wastewater and has been reported to have carcinogenic effects. The chemical structure of 3HB is similar to 2-benzoylbenzoic acid, which inhibits mitochondrial membrane potential and induces apoptosis in hamster cells. 3HB also has acute toxicities and can cause cell death by inhibiting protein synthesis or inducing DNA damage. 3HB reacts with hydrochloric acid to form benzene, which may react with saccharomyces cerevisiae strain to form benzopyrene, a known carcinogen.</p>

<p>3-Fluorophenol is a chemical compound that has a molecular formula of C6H3F3O and a molecular weight of 121.12. It has an intramolecular hydrogen bond between the hydroxyl group and the hydrogen atom in the 3-position, which is responsible for its stability. 3-Fluorophenol can be obtained by reacting 2-benzoylbenzoic acid with diazonium salt in water in the presence of sodium trifluoroacetate (NaC(O)CF3). The reaction mechanism involves an addition reaction between the diazonium salt and 2-benzoylbenzoic acid to form an intermediate, followed by nucleophilic attack from water on the intermediate to form an alcohol product. The kinetic energy of 3-fluorophenol is activated by hydrogen bonding, which leads to its ability to react with other molecules.</p>

<p>2-Methanesulfinylaniline is a chemical compound that can be used as an arylating agent. It reacts with benzaldehyde or benzaldehydes to form benzylic alcohols. The reaction is catalyzed by acid and the regioselectivity of the reaction depends on the type of acid used. 2-Methanesulfinylaniline has been shown to be effective in the synthesis of 3-benzoylbenzoic acids, which are useful intermediates in organic chemistry.</p>

2-(3-Amino-4-Chlorobenzoyl)Benzoic Acid

<p>Applications BzATP Ammonium Salt is a selective P2X purinergic agonist. It is more potent than ATP at homodimeric P2X7 receptors.<br>References Cole, D., Yount, R.: J. Biol. Chem., 265, 22537 (1990); Atarashi, K., et al.: Nature, 455, 808 (2008)<br></p>

3-Phenylphthalide is a photolabile molecule that has been used as a drug for the treatment of Parkinson's disease. It is an amine and is chiral, with two stereoisomers. 3-Phenylphthalide was synthesized in order to study the mechanism of action of drugs that are metabolized by chiral amines. 3-Phenylphthalide is a competitive inhibitor of 2-benzoylbenzoic acid chloride and chloride bonds cleavage, which are important steps in the synthesis of neurotransmitters. This drug also has been shown to inhibit the metabolism of benzoate to benzoylcholine, which may contribute to its effects on the nervous system.

3-Benzoylpropanoic acid is an inhibitor of the enzyme phosphatase. It binds to the hydroxyl group of serine residues on the enzyme and prevents it from catalyzing reactions. This inhibition can lead to mitochondrial dysfunction, which may be involved in the development of autoimmune diseases such as lupus erythematosus and rheumatoid arthritis. 3-Benzoylpropanoic acid has been used successfully to treat choroidal neovascularization, a condition that causes vision loss due to abnormal blood vessel growth in the eye. The optimum pH for this drug is 7.5 and it can be broken down by a phosphatase enzyme into 2-benzoylbenzoic acid, a metabolite that is less active than 3-benzoylpropanoic acid.

1,2-Diphenoxyethane is a diphenyl ether that has been used as a carbonyl group. It is orthoboric acid-permeable and has high kinetic energy. It also has an aliphatic hydrocarbon chain that is substituted with a hydroxyl group at one end. The molecule is colorless and water-soluble in the solid state. 1,2-Diphenoxyethane can be prepared from the reaction of 2-benzoylbenzoic acid with phenol and formaldehyde. 1,2-Diphenoxyethane can be synthesized by heating 1,4-dibromo-2-butene together with sodium hydroxide to produce a mixture of 1,2-, 1,3-, and 2,3-dibromoalkenes. The viscosity of the reaction solution increases as the concentration of 1,2-diphenoxyethane increases.