Benzenes
Subcategories of "Benzenes"
- Benzamides(62 products)
- Benzoic Acids(5,475 products)
- Benzyl alcohols(1,457 products)
- Halogenated Benzenes(33,965 products)
- Phenols(2,663 products)
Found 11889 products of "Benzenes"
Ethyl 4-chlorobenzoate
CAS:Ethyl 4-chlorobenzoate is an organic compound that is a colorless liquid with a sweet odor. It has been shown to be genotoxic in the presence of impurities such as palladium-catalyzed coupling and hemolytic activity. The structure of ethyl 4-chlorobenzoate can be determined by spectrometry analyses, which show that it contains an isopropyl group and an ethyl ester group. Ethyl 4-chlorobenzoate can be synthesized efficiently using the cross-coupling reaction between chlorides and aryl halides. This synthesis follows the same mechanism as the palladium catalyzed coupling reaction, but uses chloride ions instead of palladium complexes, which are more readily available.Formula:C9H9ClO2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:184.62 g/mol2-Chloro-4-methylsulfonylbenzoic acid
CAS:2-Chloro-4-methylsulfonylbenzoic acid is a chlorinating agent that can be used to produce triketones from ketones. It is usually used as a hydrogen peroxide scavenger and a chlorinating agent in the food industry. 2-Chloro-4-methylsulfonylbenzoic acid can also be used to produce glyphosate, phosphoric acid solution, and chloride. The chlorinating property of this compound is due to its ability to form hypochlorous acid when it reacts with water. This reaction produces hypochlorite ions that are active against microorganisms by disrupting the cell membrane. 2-Chloro-4-methylsulfonylbenzoic acid can react with organic solvents such as carbon tetrachloride and optimizes the introduction of chlorine into organic compounds.Formula:C8H7ClO4SPurity:Min. 95%Color and Shape:White PowderMolecular weight:234.66 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/mol2,4-Dihydroxy-6-pentylbenzoic acid
CAS:An intermediate in the phytocannabinoid biosynthetic pathway.Formula:C12H16O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:224.25 g/mol4-Diethylamino-2-methoxybenzaldehyde
CAS:4-Diethylamino-2-methoxybenzaldehyde (4DMMB) is a protonated molecule that is able to penetrate the mitochondrial membrane due to its low charge. Once inside, 4DMMB can be reduced by electron transfer from the mitochondria's membrane potential. This reduction leads to an increase in the mitochondrial membrane potential and subsequent photophysical emissions. The introduction of 4DMMB has been shown to cause mitochondrial membrane potential changes in cells, which may lead to pathophysiologic conditions such as cancer.Formula:C12H17NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:207.27 g/mol5-Bromosalicylic acid
CAS:5-Bromosalicylic acid is a derivative of p-hydroxybenzoic acid that is used in wastewater treatment. The reaction of 5-bromosalicylic acid with the 1,3-benzodioxole-5-carboxylic acid leads to the formation of a new compound, which can be used as an intermediate in organic synthesis. 5-Bromosalicylic acid has been shown to inhibit the growth of hepg2 cells and K562 cells by damaging DNA. It also inhibits the suzuki coupling reaction by acting as a hydrogen sink and stabilizing the transition state through intramolecular hydrogen bonding interactions. A possible mechanism for this inhibition is that 5-bromosalicylic acid reacts with hydroxide ions to form bromohydroxylated products, which then react with amine compounds to produce carboxylates that can hydrogen bond with other molecules.Formula:C7H5BrO3Purity:Min. 95%Color and Shape:White PowderMolecular weight:217.02 g/mol3,5-Dinitro-4-hydroxybenzoic acid
CAS:3,5-Dinitro-4-hydroxybenzoic acid (DNHB) is an organic compound that is used as a reagent in organic synthesis. DNHB has been shown to be a nucleophile, reacting with chloride ions from HCl and forming the corresponding 3,5-dinitrosalicylic acid (DNSA) salt. This reaction has been shown to be efficient at low temperature and pH values. The efficiency of this reaction has been shown to increase by the addition of halides such as fluoride and bromide. Electrospray ionisation mass spectroscopy analysis of DNHB has also revealed that it is an anion with a molecular weight of 228.3 g/mol. DNHB is synthesised by reacting benzoic acid with nitrous acid and hydrochloric acid, followed by treatment with concentrated sulfuric acid.Formula:C7H4N2O7Purity:Min. 95%Color and Shape:Yellow PowderMolecular weight:228.12 g/mol3,5-Dichloro-2-methoxybenzoic acid
CAS:3,5-Dichloro-2-methoxybenzoic acid (3,5-DMB) is a diphenyl ether with a pharmacokinetic half-life of about 3 hours. It has two isomers: the cis and trans forms. The cis isomer is more active than the trans form. The cis isomer has been shown to be effective in treatments for amine oxidase inhibitors and short-chain fatty acids. It also has growth regulator properties that are used in treatments for psoriasis and acne. 3,5-DMB inhibits bacterial growth by binding to the enzyme dioxygenase, which catalyzes the conversion of 4-hydroxybenzoic acid into 4-hydroxyphenylpyruvic acid; this prevents the production of catecholamines and subsequent cell proliferation. This drug binds to apical membranes in the intestine by attaching to sulfhydryl groups on proteins involved in transport processes, preventing uptakeFormula:C8H6Cl2O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:221.04 g/mol4-Cyanobenzaldehyde
CAS:4-Cyanobenzaldehyde is an acid that inhibits tyrosinase, an enzyme involved in the production of melanin. It has been shown to have a strong inhibitory effect on the activity of this enzyme in a variety of biological studies. 4-Cyanobenzaldehyde is chemically stable and does not react with hydrochloric acid or water at room temperature, making it suitable for use in experiments involving these substances. This chemical also has antiinflammatory properties and can be used as a substitute for phenols in some chemical reactions. 4-Cyanobenzaldehyde is soluble in methanol and reacts with diphenolase, an enzyme involved in the synthesis of lignin, to produce benzophenone and benzoic acid. This reaction may be important for the formation of lignin during wood decomposition.Formula:C8H5NOPurity:80%Color and Shape:PowderMolecular weight:131.13 g/mol2-Chloro-4-methoxybenzoic acid
CAS:2-Chloro-4-methoxybenzoic acid is a model compound for the screening of acridones, which are a class of compounds with anticancer activity. 2-Chloro-4-methoxybenzoic acid has been shown to inhibit potassium t-butoxide efflux in cancer cells and induce multidrug resistance in cancer cells. Furthermore, it has been shown that 2-Chloro-4-methoxybenzoic acid inhibits mitoxantrone efflux in cancer cells, leading to an increase in mitoxantrone cytotoxicity. This compound is also able to induce a phenotype change from cancerous to normal and can be used as a chemotherapeutic agent against cancers.Formula:C8H7ClO3Purity:Min. 95%Color and Shape:PowderMolecular weight:186.59 g/molMethyl 4-aminobenzoate
CAS:Methyl 4-aminobenzoate is a chemical compound that is used as a fluorescence probe in the study of DNA replication. It can be used to detect the presence of viral RNA in cell culture, and has been shown to inhibit the replication of bacterial RNA. Methyl 4-aminobenzoate binds to guanine residues in DNA and forms an alkyl bond with them. This prevents the binding of other amino acids, which are essential for DNA replication. Methyl 4-aminobenzoate has also been shown to have pharmacokinetic properties that make it useful for intravenous administration and oral administration.
Formula:C8H9NO2Purity:Min. 97.5 Area-%Color and Shape:White PowderMolecular weight:151.16 g/mol3,5-Dinitro-4-hydroxybenzaldehyde
CAS:Please enquire for more information about 3,5-Dinitro-4-hydroxybenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C7H4N2O6Purity:Min. 95%Color and Shape:PowderMolecular weight:212.12 g/mol3-tert-Butyl-4-hydroxybenzoic acid
CAS:3-tert-Butyl-4-hydroxybenzoic acid is a phenolic compound that is found in the plant species of "Solanum xanthocarpum". It has antioxidant properties and has been shown to have anticancer activity in vitro. 3-tert-Butyl-4-hydroxybenzoic acid also inhibits the growth of human colon carcinoma cells. It is soluble in organic solvents and homopolymers at high temperatures, but insoluble at lower temperatures.Formula:C11H14O3Purity:Min. 95%Color and Shape:PowderMolecular weight:194.23 g/mol4-Iodobenzoic acid
CAS:4-Iodobenzoic acid is a chiral compound that can be used as a nutrient solution in the laboratory. It has been shown to be effective at removing p-hydroxybenzoic acid and 4-dimethylaminobenzoic acid from wastewater. The reaction mechanism of 4-iodobenzoic acid involves intramolecular hydrogen transfer from the hydroxyl group on the benzoic side chain to the iodine atom, which forms an intermediate that reacts with a second molecule of benzoic acid. This reaction mechanism is similar to that found in caproic acid, except for the substitution of hydrogen with iodine. The addition of sodium hypochlorite or potassium permanganate can lead to the oxidation of 4-iodobenzoic acid and its eventual decomposition into carbon dioxide and water.
Formula:C7H5IO2Purity:Min. 95%Color and Shape:PowderMolecular weight:248.02 g/mol3-Hydroxy-2-methoxybenzoic acid
CAS:3-Hydroxy-2-methoxybenzoic acid (3HMB) is a phenolic compound that is found in the heartwood of Eucalyptus trees, fruits such as apples and cherries, and some vegetables. 3HMB has been shown to inhibit tumor necrosis factor-α (TNF-α) production by proinflammatory cytokines such as IL-1β and IL-6, which are produced by cells in response to infection or tissue injury. 3HMB also inhibits the activity of tyrosol oxygenase, which converts tyrosol to vanillic acid. Vanillic acid can be converted into vanillin, an important precursor for the synthesis of pigments that give fruits their color. 3HMB has been shown to inhibit the growth of cancer cells in vitro.Formula:C8H8O4Purity:Min. 95%Color and Shape:PowderMolecular weight:168.15 g/mol5-Bromo-2-methylbenzoic acid
CAS:Intermediate in the synthesis of canagliflozin
Formula:C8H7BrO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:215.04 g/mol2-Amino-4-methoxy-benzoic acid methyl ester
CAS:2-Amino-4-methoxy-benzoic acid methyl ester is a high quality, versatile building block for the synthesis of complex compounds. It is an intermediate in the synthesis of a number of biologically active compounds and has been used as a reagent for the determination of amino acids. 2-Amino-4-methoxy-benzoic acid methyl ester is soluble in water and polar organic solvents.Formula:C9H11NO3Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:181.19 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/mol2,6-Dihydroxybenzaldehyde
CAS:2,6-Dihydroxybenzaldehyde is a chemical compound that has been used as an intermediate in the synthesis of other chemicals. It is also used as a precursor for benzaldehyde and benzoic acid. 2,6-Dihydroxybenzaldehyde can be synthesized by reacting sodium carbonate with pluronic F127 in the presence of cationic surfactant. The surface methodology used in this process involves the use of hydrophobic molecules to form micelles and liposomes on the surface of the electrode. The interaction between these micelles and liposomes is pH dependent. This reaction causes an increase in hydrogen ions, which leads to an increase in conductivity at acidic pH values. Electrochemical impedance spectroscopy (EIS) results show that 2,6-dihydroxybenzaldehyde reacts with high concentrations of salt and water vapor. FTIR spectroscopy shows that it has two hydroxyl groups and one double
Formula:C7H6O3Purity:Min. 95%Color and Shape:PowderMolecular weight:138.12 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/mol
