
Acides benzoïques
5475 produits trouvés pour "Acides benzoïques"
2,6-Dihydroxy-4-methylbenzoic acid
CAS :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.Formule :C8H8O4Degré de pureté :Min. 98 Area-%Couleur et forme :SolidMasse moléculaire :168.15 g/mol3,5-Dihydroxy-4-methylbenzoic acid methyl ester
CAS :3,5-Dihydroxy-4-methylbenzoic acid methyl ester is a fine chemical that is used as a versatile building block in the synthesis of pharmaceuticals, agrochemicals and other chemicals. It can be used as an intermediate in the synthesis of organic compounds and research chemicals. This compound is also used as a reaction component in organic syntheses and is often found in speciality chemicals. 3,5-Dihydroxy-4-methylbenzoic acid methyl ester is soluble in most solvents and has high purity. It is a complex compound that can be used as a useful building block or reagent for many different reactions.
Formule :C9H10O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :182.17 g/mol2,3,4-Trimethoxybenzoic acid
CAS :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.Formule :C10H12O5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :212.2 g/molMethyl 4-amino-2-methyl benzoate
CAS :Methyl 4-amino-2-methyl benzoate is a fine chemical that can be used as a building block for research chemicals, pharmaceuticals, and speciality chemicals. Methyl 4-amino-2-methyl benzoate is a versatile building block in organic synthesis because it can be used as a reaction component and intermediate to synthesize other compounds. This compound is also an excellent scaffold for the synthesis of complex compounds, making it a useful intermediate for organic chemistry. Methyl 4-amino-2-methyl benzoate has CAS No. 6933-47-7 and is soluble in organic solvents such as dichloromethane, chloroform, ether, or acetone.Formule :C9H11NO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :165.19 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/mol3-Acetoxybenzoic acid
CAS :3-Acetoxybenzoic acid is a metabolite of 3-hydroxybenzoic acid, which is an intermediate in the biosynthesis of salicylic acid. It has been shown to have antibacterial properties and may be used as a topical treatment for skin infections caused by staphylococcus. 3-Acetoxybenzoic acid also has antiviral properties, which may be related to its ability to bind histone H3. 3-Acetoxybenzoic acid inhibits leishmania infantum growth and development by binding to chloride ions and preventing the formation of hydrogen bonds in the cell membrane. This prevents chloride ions from entering the cell and causes water channels to close, leading to dehydration and death.Formule :C9H8O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :180.16 g/mol4-Bromo-2-(trifluoromethyl)benzoic acid methyl ester
CAS :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%.Formule :C9H6BrF3O2Degré de pureté :Min. 95%Couleur et forme :Colorless PowderMasse moléculaire :283.04 g/molMethyl 4-bromo-2-methoxybenzoate
CAS :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.Formule :C9H9BrO3Degré de pureté :Min. 98 Area-%Couleur et forme :Yellow PowderMasse moléculaire :245.07 g/mol4,4'-Dibenzoic acid
CAS :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.Formule :C14H10O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :242.23 g/mol2-Ethoxybenzoic acid
CAS :Component in some dental cementsFormule :C9H10O3Degré de pureté :Min. 99.0 Area-%Couleur et forme :Colorless Clear LiquidMasse moléculaire :166.17 g/mol2-Amino-5-methoxybenzoic acid
CAS :2-Amino-5-methoxybenzoic acid is a useful chemical that can be used as a building block for the synthesis of more complex compounds. It has been used in the synthesis of novel pharmaceuticals and agrochemicals, as well as research chemicals. 2-Amino-5-methoxybenzoic acid is a high quality reagent that can be used in the production of fine chemicals and other specialty chemicals.Formule :C8H9NO3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :167.16 g/mol3-Dimethylaminobenzoic acid
CAS :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.Formule :C9H11NO2Degré de pureté :Min. 95%Couleur et forme :Off-White PowderMasse moléculaire :165.19 g/mol2-Amino-5-iodobenzoic acid
CAS :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
Formule :C7H6INO2Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :263.03 g/mol2-Amino-4-methoxybenzoic acid
CAS :2-Amino-4-methoxybenzoic acid is a monophenolic compound that has been shown to have antioxidant properties. It is a redox potential with a pK of 7.8 and can be protonated at the phenolic hydroxyl group. 2-Amino-4-methoxybenzoic acid has been shown to inhibit the enzyme activities of histone proteins, which are enzymes that catalyze the formation of DNA from RNA. This compound also inhibits enzymes involved in amino acid synthesis such as anthranilate synthase and malic enzyme, as well as other enzymes such as phosphotransferase (PTS) and pyruvate kinase. 2-Amino-4-methoxybenzoic acid also causes inhibition of growth in phytophthora megasperma, an oomycete plant pathogen, by altering the redox potentials inside the cell membrane. The mechanism forFormule :C8H9NO3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :167.16 g/mol2-Hydroxy-6-methylbenzoic acid
CAS :2-Hydroxy-6-methylbenzoic acid is a natural product that is synthesized by the enzyme p. pastoris. It is a member of the polyketide class of compounds and has shown to have physiological effects such as anti-inflammatory and antioxidant properties. 2-Hydroxy-6-methylbenzoic acid also has been shown to inhibit ATP binding cassette transporter (ABC) proteins, which are involved in drug resistance, from transporting drugs out of cells, making it an attractive candidate for drug discovery.
Formule :C8H8O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :152.15 g/mol3-Bromo-5-hydroxybenzoic acid
CAS :3-Bromo-5-hydroxybenzoic acid is a metabolite of 3,5-dihydroxybenzoic acid (DHB) in the metabolism of benzoic acid. It has been shown to be an antibacterial agent and has been used to treat metabolic disorders in hamsters. Symptoms of 3-bromo-5-hydroxybenzoic acid include dyslipidemia, which can lead to metabolic disorders such as diabetes mellitus and atherosclerosis. The compound may also have a role in tuberculosis and cancer due to its ability to induce apoptosis.
Formule :C7H5O3BrDegré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :217.02 g/mol3,5-Dimethylbenzoic acid
CAS :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.Formule :C9H10O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :150.17 g/mol3,5-Dibromo-4-hydroxybenzoic acid
CAS :3,5-Dibromo-4-hydroxybenzoic acid is a chemical that is used as a herbicide and insecticide. It inhibits the growth of plants by preventing protein synthesis in cells. 3,5-Dibromo-4-hydroxybenzoic acid has been found to be effective against bacteria such as Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae. The compound also has an inhibitory effect on the growth of industrial chemicals such as ethylene oxide and acetaldehyde. 3,5-Dibromo-4-hydroxybenzoic acid is produced from p-hydroxybenzoic acid by the action of corrin (a bacterial enzyme).Formule :C7H4Br2O3Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :295.91 g/molMethyl 3-amino-4-chlorobenzoate
CAS :Methyl 3-amino-4-chlorobenzoate is an analog of 3-amino-4-chlorobenzoic acid. It is a multidrug that can cross the blood brain barrier and has been shown to have cytotoxic activity in vitro. Methyl 3-amino-4-chlorobenzoate has been postulated as a possible organometallic compound and may be synthesized through a chemical diversity approach. The chloride ion, which is present in methyl 3-amino-4-chlorobenzoate, has been shown to decrease the toxicity of nitrobenzoic acid, making this compound resistant to nitrosation reactions.Formule :C8H8ClNO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :185.61 g/mol3,5-Diiodo-4-hydroxybenzoic acid
CAS :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;Formule :C7H4I2O3Degré de pureté :Min 97%Couleur et forme :PowderMasse moléculaire :389.91 g/mol
