
Acides benzoïques
5475 produits trouvés pour "Acides benzoïques"
3,5,6-Trichlorosalicylic acid
CAS :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.Formule :C7H3Cl3O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :241.46 g/mol4-Aminohippuric acid
CAS :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.Formule :C9H10N2O3Couleur et forme :PowderMasse moléculaire :194.19 g/mol2-Fluoro-4-isopropyloxybenzoic acid
CAS :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.Formule :C10H11FO3Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :198.19 g/mol4-Formyl-3-hydroxybenzoic acid
CAS :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.Formule :C8H6O4Degré de pureté :Min. 96.5 Area-%Couleur et forme :PowderMasse moléculaire :166.13 g/mol2,4-Dinitrobenzoic acid
CAS :2,4-Dinitrobenzoic acid (2,4-DNBA) is a chemical reagent that has been used as a positive control for the detection of hydrogen bonding interactions. It is also used in analytical methods to detect protonation, carboxylate, and hydroxyl groups. This compound can be prepared from picric acid by nitration with nitric acid and then reacting with aniline. The 2,4-DNBA molecule contains two intramolecular hydrogen bonds and four intermolecular hydrogen bonds. 2,4-DNBA is classified as a trifluoroacetic acid derivative.Formule :C7H4N2O6Degré de pureté :Min. 96 Area-%Couleur et forme :Slightly Yellow PowderMasse moléculaire :212.12 g/mol2-Amino-4,5-dimethoxybenzoic acid
CAS :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.Formule :C9H11NO4Degré de pureté :Min. 95%Couleur et forme :Beige PowderMasse moléculaire :197.19 g/molEthyl 4-iodobenzoate
CAS :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.Formule :C9H9IO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :276.07 g/molMethyl 4-ethylbenzoate
CAS :Methyl 4-ethylbenzoate is a molecule that has been shown to have synergistic effects with magnesium oxide, polyvinylpyrrolidone, and glycerin. It also has the ability to be used as a template molecule for the synthesis of hydrotalcite. Methyl 4-ethylbenzoate can be synthesized from ethyl benzoate and methyl iodide. It is an ingredient in some cosmetics and personal care products, such as skin lotions, hair conditioners, and fragrances. Methyl 4-ethylbenzoate has antioxidant properties due to its ability to scavenge free radicals. This compound is also used as a solvent for paints and lacquers.Formule :C11H14O2Degré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :178.23 g/molMethyl 4-amino-3-hydroxybenzoate
CAS :Methyl 4-amino-3-hydroxybenzoate is a synthetic compound that has been shown to inhibit the neuraminidase enzyme in the influenza virus. It is a ligand for the influenza virus and inhibits the release of progeny virions from infected cells. Methyl 4-amino-3-hydroxybenzoate has been shown to have antiviral effects against influenza A and B viruses in vivo and in vitro. The mechanism of action is thought to be due to its interaction with metal ion, which can reduce the availability of free water needed for viral replication.Formule :C8H9NO3Degré de pureté :Min. 95%Couleur et forme :Off-White PowderMasse moléculaire :167.16 g/mol2-tert-Butoxybenzoic acid
CAS :2-tert-Butoxybenzoic acid is a versatile chemical that can be used as a reagent, a speciality chemical, or as an intermediate in the synthesis of other compounds. It is typically used in organic chemistry for the preparation of esters, amides, and nitriles. 2-tert-Butoxybenzoic acid is also useful as a building block for complex molecules. This compound has been shown to react with alcohols to form esters, with amines to form amides, and with nitro groups to form nitriles.Formule :C11H14O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :194.23 g/mol5-Bromo-2-nitrobenzoic acid
CAS :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.
Formule :C7H4BrNO4Degré de pureté :Min. 95%Couleur et forme :Slightly Yellow PowderMasse moléculaire :246.02 g/mol2-Fluoro-4-nitrobenzoic acid methyl ester
CAS :2-Fluoro-4-nitrobenzoic acid methyl ester is a synthetic compound that has been shown to inhibit the activity of protein kinases and may be used as a lead compound for the development of allosteric inhibitors. A high yield synthesis of this compound was achieved using an allyl chloroformate, which is a versatile reagent that can be used to synthesize 2-fluoro-4-nitrobenzoic acid methyl ester. The structural analysis of this compound showed that it binds to the allosteric site on ATP binding proteins. This site is distinct from the active site and regulates ATP binding, hydrolysis, and phosphate transfer.Formule :C8H6FNO4Degré de pureté :Min. 98%Couleur et forme :White PowderMasse moléculaire :199.14 g/mol2,4-Dimethylbenzoic acid
CAS :2,4-Dimethylbenzoic acid is a white solid with the chemical formula CH3C6H2O2. It is an organic acid that can be used as a building block in organic synthesis. The functional groups of 2,4-dimethylbenzoic acid are methyl and carboxyl. The most efficient method for the synthesis of 2,4-dimethylbenzoic acid is by reacting hydrochloric acid with dimethylaniline. This reaction can be carried out in one pot without isolation of intermediates. The structural analysis of 2,4-dimethylbenzoic acid was done using fluorescence lifetimes and hydrochloric acid. The reaction mechanism for the formation of 2,4-dimethylbenzoic acid from dimethylaniline is through a nucleophilic substitution reaction with chloride ion. Sample preparation for 2,4-dimethylbenzoic acid includes dissolution in water and filtration through a 0.45Formule :C9H10O2Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :150.17 g/mol3-Iodo-4-methylbenzoic acid
CAS :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 receptorFormule :C8H7IO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :262.04 g/mol4-Bromo-3,5-dihydroxybenzoic acid methyl ester
CAS :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.Formule :C8H7BrO4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :247.04 g/mol2-Amino-5-methylbenzoic acid
CAS :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. 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.Formule :C8H9NO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :151.16 g/mol5-Fluoroanthranilic acid
CAS :5-Fluoroanthranilic acid is a synthetic compound that belongs to the class of anthranilic acid derivatives. It inhibits the growth of bacteria by reacting with the hydroxyl group on the bacterial cell wall and binding to its target, which is a cellular component found in Gram-positive bacteria. The molecular modeling and gene analysis have shown that this compound has an optimal reaction at pH 8.5, which is not in accordance with the natural environment of bacteria. 5-Fluoroanthranilic acid has been shown to have anticancer activity against wild-type cells but not against resistant mutants.Formule :C7H6FNO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :155.13 g/mol2,6-Dichloro-3,5-dihydroxybenzoic acid
CAS :2,6-Dichloro-3,5-dihydroxybenzoic acid is a reagent with a wide range of applications in the research and development of chemical products. It is also a useful intermediate for the synthesis of other compounds. 2,6-Dichloro-3,5-dihydroxybenzoic acid has been shown to be used as a building block for the synthesis of various complex compounds. It is also an important reaction component that can be used in many different reactions to produce valuable products.Formule :C7H4Cl2O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :223.01 g/mol3-Methyl-4-nitrobenzoic acid
CAS :3-Methyl-4-nitrobenzoic acid is a white solid that can be synthesized by heating 2,4-dichlorobenzoic acid with potassium dichromate in the presence of nitrogen. It has been shown to be effective against Candida glabrata strains and other bacteria. 3-Methyl-4-nitrobenzoic acid is soluble in water and other polar solvents, such as acetic acid or sodium carbonate, but insoluble in nonpolar solvents such as hexane or ether. The reaction mechanism for this compound is not yet known. It has been found to have a phase equilibrium between its solid and liquid forms at room temperature. Solubility data for this compound are available from experimental measurements.
Formule :C8H7NO4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :181.15 g/mol2-Phenoxybenzoic acid
CAS :2-Phenoxybenzoic acid is a hydrochloride salt that is used as a reagent in analytical chemistry. It reacts with the carboxylate group of amino acids, proteins, and peptides to form a stable, water-soluble complex. The reaction is typically monitored by measuring the change in optical density at 260 nm. 2-Phenoxybenzoic acid reacts with bcr-abl kinase and colloidal gold to form an insoluble precipitate that can be detected with electron microscopy. This compound also has biological properties such as inhibiting carbonic anhydrase activity and changing the pH of the solution. 2-Phenoxybenzoic acid was originally synthesized from diphenyl ether and phenol (C6H5OH). 2-Phenoxybenzoic acid can be converted into 2-(4-nitrophenoxy) benzoic acid by reacting it with sodium nitrite followed by hydrochloric acidFormule :C13H10O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :214.22 g/mol
