Benzoic Acids
Benzoic acids are aromatic carboxylic acids with the molecular formula C7H6O2, characterized by a benzene ring bonded to a carboxyl group (-COOH). These compounds are widely used as preservatives, intermediates in organic synthesis, and in the production of various chemicals, including dyes and fragrances. Benzoic acids are also important in the food and pharmaceutical industries. At CymitQuimica, we provide a diverse range of high-quality benzoic acids to support your research and industrial needs.
Found 5474 products of "Benzoic Acids"
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2-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 acidFormula:C13H10O3Purity:Min. 95%Color and Shape:PowderMolecular weight:214.22 g/mol3,5-Dibromo-2-anisic acid
CAS:3,5-Dibromo-2-anisic acid is a short chain dodecyl amine with the chemical formula CH2Br2C6H4N. It is an active compound that has been shown to have nematicidal activity and also shows high activity against saprophytes. 3,5-Dibromo-2-anisic acid is synthesized by reacting chlorine with salicylaldehyde in the presence of a base. The compound is used in the synthesis of various other organic compounds such as amides and amines.Formula:C8H6Br2O3Purity:Min. 95%Color and Shape:PowderMolecular weight:309.94 g/molMethyl 5-nitrosalicylate
CAS:Methyl 5-nitrosalicylate is a chemical compound that belongs to the group of 4-hydroxycoumarin derivatives. It is an inhibitor of the reaction between salicylic acid and nitrous acid, inhibiting the formation of 5-nitrosalicylic acid. Methyl 5-nitrosalicylate has shown inhibitory activity against various nitro compounds, including benzofurans. The inhibitory effect on oxidation reactions may be due to its ability to act as a ligand and form coordination complexes with metal ions such as copper, zinc, and iron. Methyl 5-nitrosalicylate also has anti-inflammatory properties that are due to its ability to inhibit prostaglandin synthesis by blocking cyclooxygenase enzyme activity. Methyl 5-nitrosalicylate can be synthesized in a few ways. One method includes reacting methyl salicylate with nitrous acid in the presence of lightFormula:C8H7NO5Purity:Min. 95%Color and Shape:PowderMolecular weight:197.14 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.
Formula:C8H8O3Purity:Min. 95%Color and Shape:PowderMolecular weight:152.15 g/molBenzoic acid N-hydroxysuccinimide ester
CAS:Benzoic acid N-hydroxysuccinimide ester is a chemical compound that is used for the diagnosis of cancer. It is used as a reagent in chromatographic methods and as a sample preparation agent in amine extraction techniques. The benzoate group reacts with amines to form an aminobenzoate ester, which can be detected by ionization techniques. This reaction mechanism has been studied extensively with spinorphin and epidermal growth factor.Formula:C11H9NO4Purity:Min. 95%Color and Shape:White PowderMolecular weight:219.19 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.Formula:C9H9IO2Purity:Min. 95%Color and Shape:PowderMolecular weight:276.07 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.Formula:C9H10N2O3Color and Shape:PowderMolecular weight:194.19 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 3-chlorobenzoate
CAS:Methyl 3-chlorobenzoate is a carbonyl compound that is used in the synthesis of salicylhydroxamic acid. This product has been shown to be an effective inhibitor of soil microorganisms, with the greatest inhibitory effect occurring at concentrations of 0.5 mg/L. The methyl 3-chlorobenzoate molecule contains aryl chlorides and a functional group, which can be identified using nmr spectra. Methyl 3-chlorobenzoate also has control experiments that show it does not interfere with the production of ethyl esters or benzoates from acetaldehyde and propionaldehyde respectively. Methyl 3-chlorobenzoate is synthesized by heating copper salt with an isopropyl group and ethyl esters in benzene solvent at refluxing temperature for two hours.Formula:C8H7ClO2Purity:Min. 95%Color and Shape:PowderMolecular weight:170.59 g/mol2,4,6-Trimethylbenzoic acid
CAS:2,4,6-Trimethylbenzoic acid is a molecule that belongs to the class of carboxylates. It has been shown to exhibit anticarcinogenic properties in patients with cervical cancer. 2,4,6-Trimethylbenzoic acid inhibits the growth of cervical cancer cells by blocking the activation of ferrocenecarboxylic acid (FCCA). This compound also blocks the activity of hydrogen bond and nitrogen atoms that are essential for cell division and development. 2,4,6-Trimethylbenzoic acid is used as an intermediate in the production of ferrocene derivatives. It can be used for acylation reactions with aromatic or aliphatic amines under acidic conditions.
Formula:C10H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:164.2 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
25gTo inquire50gTo inquire100gTo inquire250gTo inquire500gTo inquire-Unit-ggTo inquireEthyl 4-amino-2-nitrobenzoate
CAS:Ethyl 4-amino-2-nitrobenzoate is a chemical intermediate that is used in the synthesis of other chemicals. It is also a versatile building block with many uses, such as in the production of research chemicals or as a reagent. It has CAS No. 84228-46-6 and can be purchased from various suppliers.Formula:C9H10N2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:210.19 g/molEthyl homovanillate
CAS:Inhibitor of monoamine oxidase AFormula:C11H14O4Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:210.23 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/mol3,5-Dinitro-4-hydroxybenzoic acid
CAS:3,5-Dinitro-4-hydroxybenzoic acid (DNHB) is an organic compound that is used as a reagent in organic synthesis. DNHB has been shown to be a nucleophile, reacting with chloride ions from HCl and forming the corresponding 3,5-dinitrosalicylic acid (DNSA) salt. This reaction has been shown to be efficient at low temperature and pH values. The efficiency of this reaction has been shown to increase by the addition of halides such as fluoride and bromide. Electrospray ionisation mass spectroscopy analysis of DNHB has also revealed that it is an anion with a molecular weight of 228.3 g/mol. DNHB is synthesised by reacting benzoic acid with nitrous acid and hydrochloric acid, followed by treatment with concentrated sulfuric acid.Formula:C7H4N2O7Purity:Min. 95%Color and Shape:Yellow PowderMolecular weight:228.12 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.Formula:C9H10O2Purity:Min. 95%Color and Shape:PowderMolecular weight:150.17 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/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.Formula:C9H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:180.16 g/mol2-Hydroxy-4-methoxybenzoic acid
CAS:2-Hydroxy-4-methoxybenzoic acid (2HMB) is a natural product with tuberculostatic activity and is also used as a pharmaceutical drug. It is an enzyme inhibitor that binds to the diphenolase domain of mycobacterial cell wall hydrolases, such as lysyl oxidase and chitinase. 2HMB has been shown to be effective against cancer cells in vitro. The monosodium salt of 2HMB is more stable than the free acid form and can be used for the treatment of tuberculosis in India. 2HMB has also been shown to inhibit the growth of bacteria in human serum and tissue culture.Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 g/molMethyl 4-chlorobenzoate
CAS:Methyl 4-chlorobenzoate is a synthetic chemical that belongs to the group of phenyl compounds. It is a solvent for organic solvents and has been shown to be toxic to humans. Methyl 4-chlorobenzoate is used in various industrial applications, such as in the production of pesticides, herbicides, and pharmaceuticals. Methyl 4-chlorobenzoate can also be used as an intermediate for the synthesis of other chemicals, such as chlorinated hydrocarbons. This chemical has been reported to cause environmental pollution and has been classified as a carcinogen by the International Agency for Research on Cancer (IARC).Formula:C8H7ClO2Purity:Min. 98.5%Color and Shape:White PowderMolecular weight:170.59 g/mol
