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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3-Bromo-4-methoxybenzoic acid
CAS:3-Bromo-4-methoxybenzoic acid is a methyl ester of 3-bromo-4-methoxybenzoic acid. It is used as a reagent in organic synthesis, including the hydrolysis of esters and nitriles to acids and amines respectively. The compound is also used in the synthesis of 3-bromo-4-methoxybenzamide and other bromomethyl benzoates. The trifluoroacetic acid reacts with cuprous cyanide to form ethyl formate and methoxybenzoate, which reacts with thionyl chloride to form the chloride 3-bromo-4-methoxybenzoic acid. This compound can be demethylated by acetaldehyde or alkali metal hydroxides to give methyl formate and methanol. It can also react with acetonitrile to produce 3,3′,3″Formula:C8H7BrO3Purity:Min. 95%Color and Shape:PowderMolecular weight:231.04 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 acidFormula:C13H10O3Purity:Min. 95%Color and Shape:PowderMolecular weight:214.22 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-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/mol4-Acetylbenzoic acid
CAS:4-Acetylbenzoic acid is a reactive functional group that is used to synthesize esters and amides. It has been shown to have anticancer activity in vitro, which may be due to the disruption of basic cellular proteins involved in DNA replication. 4-Acetylbenzoic acid is soluble in neutral pH and reacts with nucleophiles such as hydroxide ions or alcohols, forming alcohols or acetates respectively. The reaction mechanism for this compound is nucleophilic attack on the carbonyl carbon, followed by loss of water from the leaving group. Significant cytotoxicity has been observed in vitro at concentrations of 2mM and higher. This effect was particularly pronounced for cells exposed to radiation or treated with 4-acetylbenzoic acid before being exposed to radiation.
Formula:C9H8O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:164.16 g/mol2-Amino-6-chlorobenzoic acid
CAS:2-Amino-6-chlorobenzoic acid is a fine chemical that is used as a reagent or speciality chemical.
Formula:C7H6ClNO2Molecular weight:171.58 g/mol3-Formyl-4-hydroxybenzoic acid
CAS:3-Formyl-4-hydroxybenzoic acid is a synthetic compound with anticancer activity. It is an azobenzene that has been shown to have photocatalytic activity. 3-Formyl-4-hydroxybenzoic acid has a carboxylate functional group and the ethyl ester functional group. The anticancer activity of this compound may be due to hydrogen bonding interactions, as well as its ability to cause DNA damage in cells by photolysis and its antiviral potency.Formula:C8H6O4Purity:90%Color and Shape:White PowderMolecular weight:166.13 g/molEthyl homovanillate
CAS:Inhibitor of monoamine oxidase AFormula:C11H14O4Purity:Min. 95%Color and Shape:Colorless PowderMolecular weight:210.23 g/molEthyl 4-bromobenzoate
CAS:Ethyl 4-bromobenzoate is a halide that can be synthesized by the cross-coupling reaction with an aryl halide and a boronic acid. This synthesis has been used successfully to prepare benzoates, which are generally more difficult to synthesize than boronic acids. The coupling reaction of ethyl 4-bromobenzoate with an aryl halide and a boronic acid in the presence of copper as catalyst yields ethyl 4-bromobenzoate in high yield. A synergistic interaction occurs between the two reagents, leading to significant cytotoxicity in vitro. This property may be due to the light emission from this compound when it is exposed to ultraviolet light. Ethyl 4-bromobenzoate is also able to inhibit aerobic glycolysis and cancer cell growth in vitro through its ability to inhibit the activity of phosphofructokinase 1 (PFK1Formula:C9H9BrO2Purity:Min. 97.5 Area-%Color and Shape:Clear LiquidMolecular weight:229.07 g/mol2,3-Dihydroxybenzoic acid
CAS:2,3-Dihydroxybenzoic acid is an antioxidant found in many plants. It has a protective effect against oxidative injury. 2,3-Dihydroxybenzoic acid has been used as a model for the study of infectious diseases and its effects on biological studies. This compound has been shown to prevent the growth of Aerobacter aerogenes and Dinucleotide phosphate. 2,3-Dihydroxybenzoic acid is also used as an ingredient in sephadex g-100 and it acts as an antimicrobial agent that prevents microbial growth in wastewater treatment systems.Formula:C7H6O4Purity:Min. 95%Color and Shape:PowderMolecular weight:154.12 g/mol2,4-Dihydroxy-3-methylbenzoic acid
CAS:2,4-Dihydroxy-3-methylbenzoic acid (2,4-DMB) is a potent compound that has been shown to have chemotherapeutic properties. It is a DNA repair agent that also inhibits the activity of topoisomerase II and DNA polymerase III. 2,4-DMB can be used in the treatment of radiation and ionizing radiation induced cancers. The pharmacophore of 2,4-DMB has been identified as being composed of three hydrophobic regions and one hydrophilic region. This pharmacophore has been used to design other potent compounds with similar activity against cancer cells.
Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 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/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/mol2,6-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.Formula:C8H8O4Purity:Min. 98 Area-%Color and Shape:SolidMolecular weight:168.15 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/mol2-Isopropylbenzoic acid
CAS:2-Isopropylbenzoic acid is a fine chemical that belongs to the group of aromatic compounds and has the molecular formula C8H10O2. This compound is used in research as an intermediate for organic synthesis, such as the production of pharmaceuticals. 2-Isopropylbenzoic acid is also a versatile building block for complex molecules, such as dyes and fragrances. It can be used as a reagent or speciality chemical in research and development, such as in polymer chemistry. 2-Isopropylbenzoic acid can be used as a reaction component for synthesis of other chemicals, such as pharmaceuticals. As an intermediate, it can be used in the production of synthetic drugs and other bioactive molecules that are difficult to synthesize by other means due to its high quality.Formula:C10H12O2Purity:Min. 95%Color and Shape:White PowderMolecular weight:164.2 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.Formula:C10H12O5Purity:Min. 95%Color and Shape:PowderMolecular weight:212.2 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.Formula:C8H8ClNO2Purity:Min. 95%Color and Shape:PowderMolecular weight:185.61 g/molEthyl 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/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.Formula:C8H9NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:167.16 g/mol
