Ácidos benzoicos
Los ácidos benzoicos son ácidos carboxílicos aromáticos con la fórmula molecular C7H6O2, caracterizados por un anillo bencénico unido a un grupo carboxilo (-COOH). Estos compuestos se utilizan ampliamente como conservantes, intermediarios en la síntesis orgánica y en la producción de diversos productos químicos, incluidos colorantes y fragancias. Los ácidos benzoicos también son importantes en las industrias alimentaria y farmacéutica. En CymitQuimica, ofrecemos una gama diversa de ácidos benzoicos de alta calidad para apoyar sus necesidades de investigación e industriales.
Se han encontrado 5474 productos de "Ácidos benzoicos"
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Methyl 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.Fórmula:C8H7NO4Pureza:Min. 95%Forma y color:Yellow Clear LiquidPeso molecular:181.15 g/mol2,4-Dinitrobenzoic acid
CAS:2,4-Dinitrobenzoic acid (2,4-DNBA) is a chemical reagent that has been used as a positive control for the detection of hydrogen bonding interactions. It is also used in analytical methods to detect protonation, carboxylate, and hydroxyl groups. This compound can be prepared from picric acid by nitration with nitric acid and then reacting with aniline. The 2,4-DNBA molecule contains two intramolecular hydrogen bonds and four intermolecular hydrogen bonds. 2,4-DNBA is classified as a trifluoroacetic acid derivative.Fórmula:C7H4N2O6Pureza:Min. 96 Area-%Forma y color:Slightly Yellow PowderPeso molecular:212.12 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.Fórmula:C9H9IO2Pureza:Min. 95%Forma y color:PowderPeso molecular:276.07 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.Fórmula:C8H8ClNO3Forma y color:White PowderPeso molecular:201.61 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-ethynylbenzaldehydeFórmula:C9H6O2Pureza:Min. 95%Forma y color:Yellow solid.Peso molecular:146.14 g/mol2-Chloro-4-trifluoromethylbenzoic acid
CAS:2-Chloro-4-trifluoromethylbenzoic acid is a chemical compound with the formula CHClFO. It can be obtained by deprotonation of 2,4,6-trichlorobenzoic acid with butyllithium and subsequent reaction with chlorotrifluoromethane. The product has two regioisomers, one in which the chlorine atom is attached to the para position on the benzene ring and the other in which it is attached to the ortho position. Substituents such as alkyl groups or lithium reagents can affect both reactivity and selectivity. The halogen substituent can also be replaced by other functional groups to make derivatives of this compound.
Fórmula:C8H4ClF3O2Pureza:Min. 95%Forma y color:PowderPeso molecular:224.56 g/mol3,5-Dichloro-4-hydroxybenzoic acid
CAS:3,5-Dichloro-4-hydroxybenzoic acid is a phenolic acid that can be found in aromatic hydrocarbons. It has been shown to have antiallergic properties and has been used as an extract to treat acute toxicities. 3,5-Dichloro-4-hydroxybenzoic acid has also been shown to inhibit the production of p-hydroxybenzoic acid by rat liver microsomes. This compound may be useful in treating high blood pressure and vascular disease. It may also be used as a natural remedy for arthritis, as it has shown antiinflammatory effects. In addition, this compound can inhibit the growth of cancer cells and stimulate the immune system by binding to monoclonal antibodies that are specific for acidic pH.Fórmula:C7H4Cl2O3Pureza:Min. 95%Forma y color:PowderPeso molecular:207.01 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.Fórmula:C9H9NO4Pureza:Min. 95%Forma y color:PowderPeso molecular:195.17 g/mol4-Hydroxybenzoic acid
CAS:4-Hydroxybenzoic acid is a plant metabolite that is found in many plants and fruits. 4-Hydroxybenzoic acid has been shown to have anti-diabetic effects in vitro. This compound also has anti-inflammatory properties, which may be due to its ability to inhibit the production of effector proteins such as nitric oxide synthase and cyclooxygenase. The biological activity of 4-hydroxybenzoic acid is dependent on the concentration; at low concentrations it inhibits glucose uptake by cells, while at high concentrations it prevents cell growth.Fórmula:C7H6O3Pureza:Min. 98 Area-%Forma y color:White Off-White PowderPeso molecular:138.12 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.Fórmula:C9H10N2O3Forma y color:PowderPeso molecular:194.19 g/mol2-tert-Butoxybenzoic acid
CAS:2-tert-Butoxybenzoic acid is a versatile chemical that can be used as a reagent, a speciality chemical, or as an intermediate in the synthesis of other compounds. It is typically used in organic chemistry for the preparation of esters, amides, and nitriles. 2-tert-Butoxybenzoic acid is also useful as a building block for complex molecules. This compound has been shown to react with alcohols to form esters, with amines to form amides, and with nitro groups to form nitriles.Fórmula:C11H14O3Pureza:Min. 95%Forma y color:PowderPeso molecular:194.23 g/mol3,5,6-Trichlorosalicylic acid
CAS:3,5,6-Trichlorosalicylic acid binds to the active site of bacterial 5-nitrosalicylic acid reductase and inhibits its activity. It is an inhibitor of proton-translocating ATPases. 3,5,6-Trichlorosalicylic acid has been shown to be effective against a variety of bacteria at low concentrations. 3,5,6-Trichlorosalicylic acid has also been shown to inhibit some physiological activities such as the light emission and chemiluminescent reaction of luciferin in fireflies. This chemical reacts with chloride ions to produce light.Fórmula:C7H3Cl3O3Pureza:Min. 95%Forma y color:PowderPeso molecular:241.46 g/mol4-Aminobenzoic acid
CAS:4-Aminobenzoic acid is a chemical compound that can be used as an antibacterial agent in wastewater treatment. It has been shown to be effective against Aerobacter aerogenes and other bacteria. 4-Aminobenzoic acid is a basic compound with an aromatic ring and four amine groups. It is often used in the synthesis of polymers, pharmaceuticals, dyes, and pigments. The polymerase chain reaction (PCR) technique uses 4-aminobenzoic acid as a cofactor for DNA synthesis. Electrochemical impedance spectroscopy (EIS) is another application of this chemical compound in which it acts as a redox mediator in the electrical circuit. 4-Aminobenzoic acid also has been shown to have toxic effects on bowel disease cells, which may be due to its ability to react with nucleophilic groups on cell surfaces or by inhibiting the production of essential proteins or enzymes within the cells
Fórmula:C7H7NO2Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:137.14 g/mol2-Ethoxybenzoic acid
CAS:Component in some dental cementsFórmula:C9H10O3Pureza:Min. 99.0 Area-%Forma y color:Colorless Clear LiquidPeso molecular:166.17 g/mol2-Benzoylbenzoic acid
CAS:2-Benzoylbenzoic acid is an organic compound with the chemical formula C6H5CO2. It is a white solid that is soluble in water, ethanol, and ether. 2-Benzoylbenzoic acid is stable at room temperature, but decomposes when heated to above 200°C. This compound can be used as a catalyst for the synthesis of polymers.
2-Benzoylbenzoic acid is used as a raw material for the production of ferrocenecarboxylic acid and ethylene diamine. The activity index of 2-benzoylbenzoic acid was found to be high (0.7) when it was tested against Streptococcus mutans and Staphylococcus aureus.Fórmula:C14H10O3Pureza:Min. 95%Forma y color:White PowderPeso molecular:226.23 g/mol4-Hydroxybenzoic acid sodium salt
CAS:4-Hydroxybenzoic acid sodium salt (4HBA) is a drug that is used in the treatment of bowel disease. It is an antimicrobial agent that has been shown to have activity against Gram-positive and Gram-negative bacteria, including Pseudomonas aeruginosa. 4HBA has also been shown to be effective in the treatment of ulcerative colitis and Crohn's disease by reducing the production of inflammatory cytokines. The mechanism of action for 4HBA is not fully understood, but it may be due to its ability to interfere with protein synthesis in bacteria, as well as inhibit antibody responses in humans. The structural biology studies on this compound have revealed that the α subunit can bind to the β subunit, which could affect its activity.Fórmula:C7H5O3NaPureza:Min. 98 Area-%Forma y color:White PowderPeso molecular:160.1 g/mol3-Chloro-5-hydroxybenzoic acid methyl ester
CAS:3-Chloro-5-hydroxybenzoic acid methyl ester is a fine chemical that can be used as a versatile building block and reaction component in the synthesis of complex compounds. It is soluble in organic solvents such as dichloromethane, chloroform, and acetone. 3-Chloro-5-hydroxybenzoic acid methyl ester has CAS No. 98406-04-3 and a molecular weight of 149. 2.Fórmula:C8H7ClO3Pureza:Min. 98 Area-%Forma y color:White Off-White PowderPeso molecular:186.59 g/mol5-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.
Fórmula:C7H4BrNO4Pureza:Min. 95%Forma y color:Slightly Yellow PowderPeso molecular:246.02 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 0.45Fórmula:C9H10O2Pureza:Min. 95%Forma y color:White PowderPeso molecular:150.17 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.Fórmula:C9H10O3Pureza:Min. 95%Forma y color:PowderPeso molecular:166.17 g/mol
