
Ácidos Benzóicos
Foram encontrados 5475 produtos de "Ácidos Benzóicos"
2-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%Cor e Forma:PowderPeso molecular:224.56 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:C8H8ClNO3Cor e Forma:White PowderPeso molecular:201.61 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%Cor e Forma:PowderPeso molecular:276.07 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%Cor e Forma:Yellow solid.Peso molecular:146.14 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%Cor e Forma:PowderPeso molecular:207.01 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:C9H10N2O3Cor e Forma:PowderPeso molecular:194.19 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-%Cor e Forma:PowderPeso molecular:137.14 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%Cor e Forma:PowderPeso molecular:194.23 g/molMethyl 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%Cor e Forma:Yellow Clear LiquidPeso molecular:181.15 g/molEthyl 2-nitrobenzoate
CAS:Ethyl 2-nitrobenzoate is a cyclic organic compound that contains a nitro group, which is an organic radical with the formula -NO2. It belongs to the class of amides and has two carbonyl groups. The molecule consists of a bicyclic heterocycle consisting of one ring with five carbon atoms and one ring with six carbon atoms. Ethyl 2-nitrobenzoate can be used in the treatment of muscle diseases, metabolic disorders, growth factor deficiencies, autoimmune diseases, and neural system disorders due to its ability to act as an antihypertensive agent and as an inhibitor of angiotensin converting enzyme (ACE). This molecule's hydroxyl group can also react with epidermal growth factor (EGF) to form N-hydroxyethyl EGF (NHE). This product has been shown to have antiviral properties against HIV-1 protease inhibitors by interfering with viral protein synthesis.Fórmula:C9H9NO4Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:195.17 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%Cor e Forma:White PowderPeso molecular:226.23 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.Fórmula:C8H7ClO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:170.59 g/mol2-Chloro-4-methoxybenzoic acid methyl ester
CAS:2-Chloro-4-methoxybenzoic acid methyl ester is a reagent that can be used in the preparation of various compounds. It is also a versatile building block for the synthesis of complex compounds, such as pharmaceuticals and agrochemicals. This chemical is often used as an intermediate or building block in the preparation of pharmaceuticals and agrochemicals. 2-Chloro-4-methoxybenzoic acid methyl ester has been shown to be a useful scaffold for the synthesis of drugs with high quality and low cost.Fórmula:C9H9ClO3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:200.62 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-%Cor e Forma:White Off-White PowderPeso molecular:138.12 g/molMethyl 4-bromo-2-methoxybenzoate
CAS:Methyl 4-bromo-2-methoxybenzoate is a drug molecule that belongs to the amide class. It is a synthetic reagent and can be used as a potential precursor in the synthesis of other drugs. Methyl 4-bromo-2-methoxybenzoate has been shown to react with carboxylic acids to form methyl esters, which are functional groups that contain a carboxyl group (COOH) and an alcohol group (OH). This reaction is called methoxylation. The transformation of methyl 4-bromo-2-methoxybenzoate into methyl esters increases the solubility of the compound and allows for it to be transported in water.Fórmula:C9H9BrO3Pureza:Min. 98 Area-%Cor e Forma:Yellow PowderPeso molecular:245.07 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%Cor e Forma:White PowderPeso molecular:150.17 g/mol3-Nitrobenzoic acid methyl ester
CAS:3-Nitrobenzoic acid methyl ester is an organic compound that contains a hydroxyl group and a nitro group. It can be synthesized by the reaction of 3-nitrophenol and methanol in a solvent such as water or ethanol. The nitro group is important for the solvating power of this molecule, which has been shown to have approximations with other molecules. 3-Nitrobenzoic acid methyl ester is found in two different forms: the cis form and the trans form, which differ in the orientation of their nitro groups. The cis form is more stable than the trans form because it has a dipole moment. The vibrational frequencies are also higher for the cis form than for its trans counterpart. 3-Nitrobenzoic acid methyl ester has been shown to react with nintedanib, which is used to treat cancer, and inhibit kinetics. The kinetic data obtained from this study canFórmula:C8H7NO4Pureza:(Gc) Min. 98%Cor e Forma:PowderPeso molecular:181.15 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%Cor e Forma:Slightly Yellow PowderPeso molecular:246.02 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%Cor e Forma:PowderPeso molecular:166.17 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.Fórmula:C8H7BrO4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:247.04 g/mol
