
Benzoic Acids
Found 5475 products of "Benzoic Acids"
Ethyl 3-hydroxybenzoate
CAS:Ethyl 3-hydroxybenzoate is a preservative that has been shown to be effective against a variety of microorganisms, including gram-positive and gram-negative bacteria. It has been shown to bind with iron, which prevents it from interacting with tyrosinase, an enzyme necessary for the production of melanin. Ethyl 3-hydroxybenzoate also inhibits the activity of benzodiazepine receptor, which reduces the effects of benzodiazepines in the brain. This compound is used in some cosmetics as an antimicrobial agent and cosmetic preservative. The molecular descriptors for this compound are: Molecular Weight=165.07; Log P=0.5; H-bond acceptor count=3; H-bond donor count=2; rotatable bond count=2; hydrogen bond acceptor count=1; hydrogen bond donor count=2; polar surface area=79.90 Å2Formula:C9H10O3Purity:Min. 98.5 Area-%Color and Shape:White PowderMolecular weight:166.17 g/molMethyl 4-(N-methylamino)benzoate
CAS:Methyl 4-(N-methylamino)benzoate is a substance that inhibits the enzyme DPP-4, which is involved in blood glucose regulation. It has been shown to be effective against certain types of cancer and impurities that may be present in the drug. Methyl 4-(N-methylamino)benzoate is an acidic compound with molecular descriptors that include acidic and amines. This compound also has genotoxic impurities, such as benzofurans, which may affect its efficacy.Formula:C9H11NO2Purity:90%Color and Shape:PowderMolecular weight:165.19 g/mol3,5-Dimethyl-4-nitrobenzoic acid
CAS: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.Formula:C9H9NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:195.17 g/mol4-Benzyloxybenzoic acid
CAS:4-Benzyloxybenzoic acid is a carboxylic acid that is structurally related to adenosine. It has been shown to bind to the group P2 adenosine receptor, which may be involved in the regulation of locomotor activity and photophysical properties. This compound also inhibits fatty acid biosynthesis and has inhibitory effects on nerve injury, amide formation, and benzoate degradation. It has been reported that 4-Benzyloxybenzoic acid binds to metal ions such as cobalt and manganese, which may be important for its antimycobacterial activity.
Formula:C14H12O3Purity:Min. 95%Color and Shape:PowderMolecular weight:228.24 g/molMethyl 5-chlorosalicylate
CAS:Methyl 5-chlorosalicylate is a chemical compound with the molecular formula CHClO. It is a colorless liquid that has a minty odor. Methyl 5-chlorosalicylate is used in organic chemistry as an intermediate to synthesize other compounds, and it can be used in the synthesis of β-cell receptor antagonists. This drug is an analog of salicylic acid and its anti-inflammatory effects are due to the inhibition of chloride channels on macrophages. The drug's neutralizing properties have been shown by experiments with neutralizing antibody levels at physiological levels, which blocks viral replication and prevents cell damage by free radicals.Formula:C8H7ClO3Purity:Min. 95%Color and Shape:White PowderMolecular weight:186.59 g/mol4-Hydroxy-3,5-dimethylbenzoic acid
CAS: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.Formula:C9H10O3Purity:Min. 95%Color and Shape:PowderMolecular weight:166.17 g/mol3-Amino-2-hydroxybenzoic acid
CAS:3-Amino-2-hydroxybenzoic acid (AAHB) is a nonsteroidal anti-inflammatory drug that belongs to the group of pharmaceutical preparations. It inhibits the enzyme dehydroascorbate reductase, which is involved in the production of hydrogen peroxide and other reactive oxygen species by phagocytes. Hydrogen peroxide and other reactive oxygen species can cause DNA damage and lead to cancer development. AAHB may also have antimicrobial effects, as it has been shown to inhibit bacterial growth and cell adhesion. AAHB interacts with fatty acids in a similar manner as aspirin does, but with a lower potency. It has been shown to inhibit prostaglandin synthesis by inhibiting lipoxygenase activity. The binding of AAHB at these sites prevents the formation of arachidonic acid from linoleic acid and blocks the conversion of arachidonic acid into prostaglandin H2 (PGH2).Formula:C7H7NO3Purity:Min. 98 Area-%Color and Shape:Off-White PowderMolecular weight:153.14 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).Formula:C7H4Br2O3Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:295.91 g/molMethyl 4-acetylbenzoate
CAS:Methyl 4-acetylbenzoate is a synthetic compound that can be used for the synthesis of imatinib and other pharmaceuticals. It is an effective method for the synthesis of butyric acid with high enantiomeric purity. The cross-coupling reaction was first reported by Suzuki in 1979, which has been widely applied to organic synthesis because it is efficient and produces simple byproducts. This reaction has also been used in the synthesis of model compounds and natural products, as well as in environmental pollution studies.Formula:C10H10O3Purity:Min. 95%Color and Shape:PowderMolecular weight:178.18 g/mol2-Chloro-3,5-dihydroxybenzoic acid
CAS: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.Formula:C7H5ClO4Purity:Min. 90%Color and Shape:PowderMolecular weight:188.56 g/mol4-Amino-5-chloro-2-methoxybenzoic acid
CAS: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.Formula:C8H8ClNO3Color and Shape:White PowderMolecular weight:201.61 g/mol2,4-Dimethoxybenzoic acid
CAS: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.Formula:C9H10O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:182.17 g/mol2-Amino-5-iodobenzoic acid
CAS:Please enquire for more information about 2-Amino-5-iodobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formula:C7H6INO2Molecular weight:263.04 g/mol3-Nitrobenzoic acid methyl ester
CAS: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 canFormula:C8H7NO4Purity:(Gc) Min. 98%Color and Shape:PowderMolecular weight:181.15 g/mol4-Fluoro-3-hydroxybenzoic acid
CAS: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.Formula:C7H5FO3Purity:Min. 95%Color and Shape:White PowderMolecular weight:156.11 g/mol3-Hydroxy-2-methoxybenzoic acid
CAS: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.Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 g/mol5-Bromo-2-methylbenzoic acid
CAS:Intermediate in the synthesis of canagliflozin
Formula:C8H7BrO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:215.04 g/mol3,5-Diisopropyl-4-hydroxybenzoic acid
CAS: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.Formula:C13H18O3Purity:Min. 95%Color and Shape:PowderMolecular weight:222.28 g/mol3-Chloro-5-hydroxybenzoic acid ethyl ester
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
Formula:C9H9ClO3Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:200.62 g/mol2-(Bromomethyl)benzoic acid
CAS:2-(Bromomethyl)benzoic acid is a functional group that can be found in many organic compounds. It is a derivative of phthalic acid and has some similar properties, including the ability to form micelles and radical species. 2-(Bromomethyl)benzoic acid has been shown to react with carbon tetrachloride or terephthalic acid to produce peroxides. This reaction is initiated by oxidation of the carbon-carbon double bond, which produces a radical pair that reacts with oxygen in the air to form radicals that are stabilized by resonance. 2-(Bromomethyl)benzoic acid also reacts with an inorganic base such as sodium hydroxide or potassium hydroxide to produce bromine gas and water.Formula:C8H7BrO2Purity:Min. 97 Area-%Color and Shape:White Off-White PowderMolecular weight:215.04 g/molBis(2-ethylbutyl)phthalate
CAS:Bis(2-ethylbutyl)phthalate (BEBP) is a chemical that has been used in the production of polyvinyl chloride (PVC) plastics, and as a stabilizer for PVC resins. BEBP is found in low levels in human tissue samples and sediments. Levels of BEBP have been measured through gas chromatography-mass spectrometry and liquid chromatography-mass spectroscopy methods. The environmental concentrations of BEBP can be calculated using the linear regression equation. Biota are also exposed to this chemical, which may be due to its use as an additive in certain food packaging materials.Formula:C20H30O4Purity:Min. 95%Color and Shape:Colourless To Pale Yellow LiquidMolecular weight:334.45 g/moln-Heptyl 4-hydroxybenzoate
CAS:n-Heptyl 4-hydroxybenzoate is a preservative and antimicrobial agent that is used in cosmetics, pharmaceuticals, and food. It is primarily used to inhibit the growth of bacteria and fungi. The mechanism by which heptyl 4-hydroxybenzoate inhibits the growth of microorganisms is not well understood. It has been shown to be an effective inhibitor of Gram-positive bacteria such as Bacillus subtilis, but not against Gram-negative bacteria such as Escherichia coli. Heptyl 4-hydroxybenzoate has been shown to have no effect on the growth of probiotic bacteria such as Lactobacillus acidophilus. The chemical structure of n-heptyl 4-hydroxybenzoate includes a glycol ether moiety and two parabens that are linked by hydrogen bonds. These bonds can be broken by enzymes found in rat liver microsomes, leading to the release of n-Formula:C14H20O3Purity:Min. 95%Color and Shape:White Off-White PowderMolecular weight:236.31 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.
Formula:C7H5O3BrPurity:Min. 95%Color and Shape:White PowderMolecular weight:217.02 g/mol3,4-Dihydroxy-5-methoxybenzoic acid
CAS: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.Formula:C8H8O5Purity:Min. 95%Color and Shape:PowderMolecular weight:184.15 g/mol3,5-Dihydroxybenzoic acid methyl ester
CAS:3,5-Dihydroxybenzoic acid methyl ester is a potent tyrosinase inhibitor that has been shown to be effective in inhibiting the production of melanin. 3,5-Dihydroxybenzoic acid methyl ester is an active ingredient in skin lightening products and has been shown to be more potent than kojic acid, arbutin and ascorbic acid. The reaction mechanism of 3,5-Dihydroxybenzoic acid methyl ester is stepwise with hydroxybenzoic acid (HBA) being the first substrate. HBA reacts with iron oxides to form a ferric hydroxide intermediate that undergoes gelation reactions with chloride ions. This results in a molecule containing three ether linkages, which are responsible for its inhibitory activity on the enzyme tyrosinase.
Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 g/molGallic acid anhydrous
CAS:Gallic acid anhydrous is a compound that is found in plants and has antioxidant properties. Gallic acid anhydrous can be used as a model system for the study of electrochemical impedance spectroscopy. It has shown to have anti-cancer activity in vitro, but not in vivo, against squamous carcinoma cells. In addition, gallic acid anhydrous has been shown to inhibit oral pathogens and to scavenge anion radicals. Gallic acid anhydrous may have structural similarities to procyanidin B4, which is important for its antioxidant activity.Formula:C7H6O5Purity:Min. 99 Area-%Color and Shape:White PowderMolecular weight:170.12 g/mol2-(4'-Chlorobenzoyl)benzoic acid
CAS:2-(4'-Chlorobenzoyl)benzoic acid (2-CBA) is a sulfa drug that inhibits bacterial growth by blocking the synthesis of folic acid. It is also known to be luminescent and can be used in techniques such as luminescent probes. 2-CBA has antibacterial activity and can inhibit bacterial growth in a chromatographic method. 2-CBA is chemically stable and has been shown to have antibacterial properties against gram-positive bacteria, including Bacillus subtilis and Staphylococcus aureus. 2-CBA also has the ability to react with phthalazinone, an inhibitor of glutamine synthetase, which is involved in the production of ATP from ADP. This reaction results in the formation of an unstable intermediate which decomposes into CO2 and benzoic acid.
Formula:C14H9ClO3Purity:Min. 95%Color and Shape:White PowderMolecular weight:260.67 g/mol3,4-Dihydroxybenzoic acid
CAS:Dietary polyphenolFormula:C7H6O4Purity:Min. 95%Color and Shape:PowderMolecular weight:154.12 g/mol5-Carboxyvanillic acid
CAS: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.Formula:C9H8O6Purity:Min. 95%Color and Shape:PowderMolecular weight:212.16 g/mol2-Methoxy-4-aminobenzoic acid
CAS: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.Formula:C8H9NO3Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:167.16 g/molEthyl 2-methoxybenzoate
CAS: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.Formula:C10H12O3Purity:Min. 95%Color and Shape:PowderMolecular weight:180.2 g/mol5-Amino-2-nitrobenzoic acid
CAS:5-Amino-2-nitrobenzoic acid is a useful chemical building block that is used in the synthesis of complex compounds and useful scaffolds.
Formula:C7H6N2O4Molecular weight:182.13 g/molRef: 3D-A-6800
-Unit-ggTo inquire25gTo inquire50gTo inquire100gTo inquire250gTo inquire500gTo inquireMethyl 2-nitrobenzoate
CAS: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.Formula:C8H7NO4Purity:Min. 95%Color and Shape:Yellow Clear LiquidMolecular weight:181.15 g/molGlyceryl-4-aminobenzoate monomer
CAS:Glyceryl-4-aminobenzoate monomer is a fine chemical that is an important building block in the synthesis of a variety of complex compounds. It has been used as a reagent and intermediate in research and development of pharmaceuticals and agrochemicals. Glyceryl-4-aminobenzoate monomer is a versatile building block, which can be used to form polymers, coatings, adhesives, elastomers, polyurethanes, and more. The compound also has been shown to have anticancer activity against human breast cancer cells.
Formula:C10H13NO4Purity:Min. 75 Area-%Color and Shape:Off-white to beige solid.Molecular weight:211.21 g/molMethyl 3,5-dibromo-4-methylbenzoate
CAS:Methyl 3,5-dibromo-4-methylbenzoate is a versatile building block that can be used as a reagent or a speciality chemical. It is a high quality compound with many applications in research and synthesis. Methyl 3,5-dibromo-4-methylbenzoate is an intermediate in the manufacturing of polymers and pharmaceuticals. It is also a reaction component for the preparation of complex compounds, such as methyl 3,5-dimethoxybenzoate. Methyl 3,5-dibromo-4-methylbenzoate has been shown to be useful as a scaffold for the synthesis of novel compounds.
Formula:C9H8Br2O2Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:307.97 g/mol5-Nitrosalicylic acid
CAS:5-Nitrosalicylic acid is an ethylene diamine derivative that is used in organic synthesis. It reacts with nitrogen atoms to form stable complexes. 5-Nitrosalicylic acid reacts with hydrogen and forms a protonated acid complex, which is more soluble in water than the molecule itself. The protonated acid complex can be used for the production of glycan, which are biomolecules that play a major role in the human body. Synchronous fluorescence spectroscopy has shown that 5-nitrosalicylic acid reacts with glycan by hydrogen bonding interactions and stabilizing nitro groups.
Formula:C7H5NO5Purity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:183.12 g/molMethyl 4-hydroxy-2-methylbenzoate
CAS: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.Formula:C9H10O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:166.17 g/molEthyl 4-(N,N-diethylamino)benzoate
CAS: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.Formula:C13H19NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:221.3 g/mol2-Ethynylbenzoic acid
CAS: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-ethynylbenzaldehydeFormula:C9H6O2Purity:Min. 95%Color and Shape:Yellow solid.Molecular weight:146.14 g/molEthopabate - Technical
CAS: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.Formula:C12H15NO4Purity:Min. 95%Color and Shape:White PowderMolecular weight:237.25 g/mol3-Methoxybenzoic acid
CAS: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.Formula:C8H8O3Purity:Min. 95%Color and Shape:PowderMolecular weight:152.15 g/molMethyl 4-acetamido-2-methoxybenzoate
CAS: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.Formula:C11H13NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:223.23 g/mol2-Chloro-6-fluorobenzoic acid
CAS: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.Formula:C7H4ClFO2Purity:Min. 95%Color and Shape:PowderMolecular weight:174.56 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 forFormula:C8H9NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:167.16 g/mol2-Hydroxy-3-methoxybenzoic acid
CAS:2-Hydroxy-3-methoxybenzoic acid is a chemical compound that has been studied for its potential use in the treatment of prostate cancer. It is a coordination complex that binds to DNA and inhibits the process of transcription. This compound also possesses anti-inflammatory properties, which are related to its ability to inhibit prostaglandin synthesis. 2-Hydroxy-3-methoxybenzoic acid has been shown to have an effect on human HL60 cells, which may be due to its ability to induce apoptosis. This compound has also been shown to have a high degree of metabolic stability and is not toxic to normal cells at doses up to 100 μM.Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 g/mol2,6-Dimethoxybenzoic acid
CAS:2,6-Dimethoxybenzoic acid is a chemical compound with the molecular formula of C9H8O4. It belongs to the group of sesquiterpene lactones and has been shown to have anti-inflammatory properties. 2,6-Dimethoxybenzoic acid exhibits a carboxylate reaction mechanism that can be activated by an enzyme, curculigoside, which hydrolyzes the ester bond in 2,6-dimethoxybenzoic acid. The reaction mechanism involves the group p2 (COOH) on 2,6-dimethoxybenzoic acid reacting with an alcohol on curculigoside to form an ester and protocatechuic acid. The dianthus caryophyllus plant produces 2,6-dimethoxybenzoic acid as a byproduct of its synthesis of protocatechuic acid. This compound is chemically studied using solid phase microextractionFormula:C9H10O4Purity:Min. 95%Color and Shape:PowderMolecular weight:182.17 g/mol2-Amino-4,6-dimethoxybenzoic acid
CAS:2-Amino-4,6-dimethoxybenzoic acid is an organic chemical compound that can be used as a building block for the synthesis of other compounds. 2-Amino-4,6-dimethoxybenzoic acid has a number of uses including being a reagent in organic and inorganic reactions, such as the synthesis of dyes, pharmaceuticals, and pesticides. It is also used as a building block for complex compounds that are difficult to make. This chemical has been classified by the Chemical Abstract Services (CAS) registry with CAS number 21577-57-1.
Formula:C9H11NO4Purity:Min. 95%Color and Shape:Yellow SolidMolecular weight:197.19 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.Formula:C8H6FNO4Purity:Min. 98%Color and Shape:White PowderMolecular weight:199.14 g/mol3-Methyl-2-nitrobenzoic acid
CAS:3-Methyl-2-nitrobenzoic acid is a chemical that can be used for wastewater treatment. It has been shown to be effective against chlorantraniliprole, a pesticide that is often found in wastewater. 3-Methyl-2-nitrobenzoic acid also has the ability to reduce chloride levels by oxidizing it to produce chloride ions and nitrogen gas. This chemical can be used as an oxidation catalyst in wastewater treatment. 3-Methyl-2-nitrobenzoic acid has been shown to have photocatalytic activity with titanium dioxide and copper sulfate (CuSO4) under visible light illumination conditions.Formula:C8H7NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:181.15 g/mol3-Methoxy-2,4,5-trifluorobenzoic acid
CAS: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.
Formula:C8H5F3O3Purity:Min. 95%Color and Shape:White to off-white solid.Molecular weight:206.12 g/mol
