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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3-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-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/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/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/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/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/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/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/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-Bromo-2,6-dimethoxybenzoic acid
CAS:3-Bromo-2,6-dimethoxybenzoic acid is a synthetic chemical used to introduce insulators into the DNA molecule. It is also used as a treatment method for introducing branched-chain scripts into the DNA molecule. 3-Bromo-2,6-dimethoxybenzoic acid has been shown to counteract synthetic techniques, such as transistors, and can be used in plant physiology research.Formula:C9H9BrO4Purity:Min. 95%Color and Shape:PowderMolecular weight:261.07 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/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/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-Hydroxybenzoic acid
CAS:3-Hydroxybenzoic acid is a ferroelectric compound that can be found in water vapor, plants, and bacteria. It has been shown to have structural properties that are very similar to those of p-hydroxybenzoic acid. The redox potential of 3-hydroxybenzoic acid is around -0.8 volts versus the standard hydrogen electrode (p-hydroxybenzoic acid is -1.2 volts). 3-Hydroxybenzoic acid has been shown to inhibit some bacterial enzymes such as esterase and transaminase, but not others such as dehydrogenase or oxidoreductase. It also shows activity against fungal enzymes such as aminopeptidases and serine proteases. The compound can exist in two forms: the metastable form or a stable form. The metastable form can be obtained by crystallizing the compound from a solution containing copper chloride or x-ray diffraction data from wild type strainsFormula:C7H6O3Color and Shape:PowderMolecular weight:138.12 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/mol2,6-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.Formula:C7H4Cl2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:223.01 g/mol2-Amino-6-chlorobenzoic acid
CAS:2-Amino-6-chlorobenzoic acid is a reactive compound that can be used as an antimicrobial agent. It binds to the active site of enzymes and inhibits their function, thereby preventing bacterial growth. 2-Amino-6-chlorobenzoic acid also has acidic properties, which may be due to its ability to hydrolyze esters by acting as a dehydrating agent. This chemical is thermodynamically stable and can be synthesized from malonic acid or other compounds. The chemical reactions of 2-amino-6-chlorobenzoic acid can be followed by NMR spectroscopy, which provides the structural information about the molecule. The reaction mechanism for 2-amino-6-chlorobenzoic acid is similar to that of amides.Formula:C7H6ClNO2Purity:Min. 95%Color and Shape:PowderMolecular weight:171.58 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
