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 5475 products of "Benzoic Acids"
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5-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.
Formula:C7H4BrNO4Purity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:246.02 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;Formula:C7H4I2O3Purity:Min 97%Color and Shape:PowderMolecular weight:389.91 g/mol3,4-Diaminobenzoic acid
CAS:3,4-Diaminobenzoic acid is a compound that is produced by the condensation of two molecules of hydrochloric acid. 3,4-Diaminobenzoic acid has been used as a reagent in the synthesis of coumarin derivatives. This chemical has been shown to be an effective proton scavenger in an optimum concentration. Benzimidazole compounds are also synthesized from 3,4-diaminobenzoic acid and have been shown to be effective against autoimmune diseases. 3,4-Diaminobenzoic acid can be used for the production of diazonium salts, which are used in the synthesis of anti-inflammatory drugs and other pharmaceuticals. The hydroxyl group on this molecule makes it chemically stable and kinetic data shows that it has high diphenolase activity.Formula:C7H8N2O2Purity:Min. 96 Area-%Color and Shape:PowderMolecular weight:152.15 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 0.45Formula:C9H10O2Purity:Min. 95%Color and Shape:White PowderMolecular weight:150.17 g/mol2,5-Dimethyl-3-nitrobenzoic acid
CAS:2,5-Dimethyl-3-nitrobenzoic acid is a versatile building block that can be used in the synthesis of a wide range of compounds. It is also an important intermediate for the synthesis of pharmaceuticals and other speciality chemicals. 2,5-Dimethyl-3-nitrobenzoic acid has been shown to be useful in the preparation of high quality fine chemicals and research chemicals. This compound has been found to be an excellent reagent for various chemical reactions.Formula:C9H9NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:195.17 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.Formula:C8H6O4Purity:Min. 96.5 Area-%Color and Shape:PowderMolecular weight:166.13 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.Formula:C9H11NO4Purity:Min. 95%Color and Shape:Beige PowderMolecular weight:197.19 g/mol3-Amino-2,4,6-triiodobenzoic acid
CAS:3-Amino-2,4,6-triiodobenzoic acid (3AIBA) is a chemical compound that is used as a contrast agent for medical imaging. It has been shown to be useful in the diagnosis of bladder cancer, and is used in the embolization of renal artery and ureteral calculi. 3AIBA functions by binding to the antigen binding sites on the tumor cells and allows visualization with X-rays. It has also been shown to be effective in reducing blood flow in tumors by blocking blood vessels with its cationic monomer. 3AIBA binds to the phosphate groups on DNA and causes crosslinking, which prevents DNA polymerase from binding with DNA. This inhibits DNA synthesis and cell division.Formula:C7H4I3NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:514.83 g/mol3-Methoxy-4-methylbenzoic acid methyl ester
CAS:3-Methoxy-4-methylbenzoic acid methyl ester is a potent inhibitor of the neurotoxic effects of β-amyloid peptide (Aβ) on cultured human neurons. 3-Methoxy-4-methylbenzoic acid methyl ester inhibits fibrillation in vitro and fluorescence assay, suggesting that it may be a promising therapeutic agent for Alzheimer's disease. The fluorescence assay is based on the inhibition of fluorescence by 3-methoxy-4-methylbenzoic acid methyl ester, which competes with Aβ for binding to an acceptor molecule. This inhibition can be used as a marker to measure the amount of Aβ present in vivo.Formula:C10H12O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:180.2 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.Formula:C8H7BrO4Purity:Min. 95%Color and Shape:PowderMolecular weight:247.04 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/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.Formula:C11H14O2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight: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.Formula:C8H9NO3Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:167.16 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.
Formula:C8H7NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:181.15 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/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/mol4-Azidobenzoic acid
CAS:Please enquire for more information about 4-Azidobenzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C7H5N3O2Purity:Min. 97 Area-%Color and Shape:PowderMolecular weight:163.13 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.Formula:C8H9NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:151.16 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 receptorFormula:C8H7IO2Purity:Min. 95%Color and Shape:PowderMolecular weight:262.04 g/mol2,5-Dichlorobenzoic acid ethyl ester
CAS:2,5-Dichlorobenzoic acid ethyl ester is a high quality, versatile building block that can be used as a reagent or intermediate. It is a useful scaffold for the synthesis of fine chemicals and research chemicals. This compound has been used in the synthesis of 2,5-dichloro-N-(2-hydroxyethyl)benzamide (CAS No. 35112-27-7), which is a speciality chemical with potential applications in pharmaceuticals and agrochemicals. 2,5-Dichlorobenzoic acid ethyl ester reacts with an amine to produce an N-[2-(2,5-dichlorophenyl)ethyl]amine (CAS No. 35112-27-7). The reaction proceeds via an amide bond formation by condensation of the amine with the acid chloride formed from the acid and ethyl chloride. This reaction is facilitated by heat andFormula:C9H8Cl2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:219.06 g/mol
