Benzenes
Benzenes are simple aromatic hydrocarbons consisting of a six-membered carbon ring with alternating double bonds. This fundamental structure is a building block for numerous chemical compounds, including pharmaceuticals, polymers, and dyes. Benzenes are used extensively in organic synthesis due to their stability and versatility. At CymitQuimica, we provide a broad range of high-quality benzenes to support your research and industrial applications.
Subcategories of "Benzenes"
- Benzamides(62 products)
- Benzoic Acids(5,474 products)
- Benzyl alcohols(1,458 products)
- Halogenated Benzenes(33,965 products)
- Phenols(2,664 products)
Found 11888 products of "Benzenes"
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5-Fluoro-2-methylbenzoic acid
CAS:5-Fluoro-2-methylbenzoic acid is a synthetic compound that has antiviral potency against the influenza A virus. It is the active form of 5-fluoro-2-methylbenzoyl chloride, which is synthesized from a Grignard reagent and an asymmetric synthesis. 5-Fluoro-2-methylbenzoic acid has been shown to have anticancer properties in vitro, which may be due to its ability to inhibit cancer cell growth through interaction with chloride channels. This drug also inhibits the activity of dehydrogenases, which are enzymes that catalyze the oxidation of various substrates by reducing them.Formula:C8H7FO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:154.14 g/mol2-Amino-6-methoxybenzonitrile
CAS:2-Amino-6-methoxybenzonitrile is an organic compound that belongs to a group of monosubstituted hydroxylamines. It has been used in the synthesis of various analogues, such as caprolactam and methoxyanthranilic acid. Hydrochloric acid reacts with 2-amino-6-methoxybenzonitrile to form 2-amino-6-hydroxybenzonitrile, which can be oxidized to 2-amino-6-(hydroxymethyl)benzonitrile. This reaction is catalyzed by copper or zinc metal.Formula:C8H8N2OPurity:Min. 95%Color and Shape:PowderMolecular weight:148.16 g/mol3,4-Dibenzyloxybenzaldehyde
CAS:3,4-Dibenzyloxybenzaldehyde is a chemical compound with the formula ClCH=C(O)CHO. This compound is an intermediate in the synthesis of the cancer drug daunorubicin. 3,4-Dibenzyloxybenzaldehyde has been shown to induce apoptosis in human ovary cells and has been detected in urine samples from patients undergoing chemotherapy for ovarian cancer. 3,4-Dibenzyloxybenzaldehyde also inhibits the production of flavonoids and has been shown to inhibit rat striatal membranes and rat atria.
Formula:C21H18O3Purity:Min. 95%Color and Shape:PowderMolecular weight:318.37 g/mol2,5-Dimethoxybenzaldehyde
CAS:Intermediate in organic synthesis
Formula:C9H10O3Purity:Min. 98 Area-%Color and Shape:Off-White PowderMolecular weight:166.17 g/molα-Sulfophenylacetic acid
CAS:Alpha-Sulfophenylacetic acid is a high quality reagent that is useful as an intermediate in the synthesis of complex compounds. It is also a fine chemical that can be used as a building block for the synthesis of speciality chemicals and research chemicals. Alpha-sulfophenylacetic acid is a versatile building block for reactions involving organic synthesis, and can be used as a reaction component to produce dyes, pharmaceuticals, pesticides, and herbicides.Formula:C8H8O5SPurity:Min. 95.0 Area-%Molecular weight:216.21 g/molRef: 3D-S-9630
1kgTo inquire5kgTo inquire10kgTo inquire25kgTo inquire2500gTo inquire-Unit-kgkgTo inquire3-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/mol3,4-Dihydroxybenzoic acid
CAS:Dietary polyphenolFormula:C7H6O4Purity:Min. 95%Color and Shape:PowderMolecular weight:154.12 g/mol3-(Trifluoromethyl)phenylacetone
CAS:3-(Trifluoromethyl)phenylacetone is a chiral iminium-type organocatalyst that is used in asymmetric organic reactions. This compound has been shown to be effective for the synthesis of chiral amines and hydroxyl groups, as well as biotransformations. 3-(Trifluoromethyl)phenylacetone binds to substrates through hydrogen bonding, steric interactions, and electrostatic interactions. It also has a high affinity for hydroxides and isosteres. 3-(Trifluoromethyl)phenylacetone can be used as an alternative to L-proline in certain biotransformations because it binds more tightly to the enzyme than L-proline does.
Formula:C10H9F3OPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:202.17 g/molBenzoic acid N-hydroxysuccinimide ester
CAS:Benzoic acid N-hydroxysuccinimide ester is a chemical compound that is used for the diagnosis of cancer. It is used as a reagent in chromatographic methods and as a sample preparation agent in amine extraction techniques. The benzoate group reacts with amines to form an aminobenzoate ester, which can be detected by ionization techniques. This reaction mechanism has been studied extensively with spinorphin and epidermal growth factor.Formula:C11H9NO4Purity:Min. 95%Color and Shape:White PowderMolecular weight:219.19 g/mol3-Fluoro-4-hydroxybenzaldehyde
CAS:3-Fluoro-4-hydroxybenzaldehyde is a hydroxyl group with an activation energy of 87.7 kJ/mol. The molecule can be synthesized by the reaction of salicylaldehyde and 3,4-dihydroxybenzaldehyde in the presence of an organic solvent such as chloroform or methylene chloride. This compound has been shown to cause cell death in ht-29 cells and cancer cell lines, as well as human ovarian carcinoma cells. It causes apoptosis by inhibiting mitochondrial membrane potential, which leads to decreased intracellular ATP levels. 3-Fluoro-4-hydroxybenzaldehyde is most commonly used in molecular modeling studies to represent the hydroxyl group due to its simplicity in comparison to other hydroxyl groups like methanol or ethanol.Formula:C7H5FO2Purity:90%Color and Shape:White PowderMolecular weight:140.11 g/mol1,3-Diphenylacetone
CAS:1,3-Diphenylacetone is a redox potential polymer that is soluble in organic solvents and is used as a film-forming polymer. It has been shown to have some intramolecular hydrogen bonding between the ketone and the nitrogen atoms, which can be seen in its chemical structure. The FTIR spectra of this compound show that it has a hydroxyl group and gives off water vapor when heated. 1,3-Diphenylacetone is an excellent solvent for detergents because it does not corrode metals or rubber. This molecule also has a basic structure due to its benzyl groups.Formula:C15H14OPurity:Min. 95%Color and Shape:PowderMolecular weight:210.28 g/mol4-Methoxybenzoic acid hydrazide
CAS:4-Methoxybenzoic acid hydrazide is a copper complex that binds to the DNA of bacteria, inhibiting the production of proteins. It has been shown to have antimicrobial activity against gram-positive and gram-negative bacteria. 4-Methoxybenzoic acid hydrazide has also been shown to inhibit colorectal carcinoma cells in vitro and in vivo. This compound inhibits the growth of cells by binding to them and disrupting hydrogen bonds. 4-Methoxybenzoic acid hydrazide causes cell death by inhibiting protein synthesis.Formula:C8H10N2O2Purity:Min. 95%Color and Shape:White PowderMolecular weight:166.18 g/mol3-Amino-4-methylbenzonitrile
CAS:3-Amino-4-methylbenzonitrile is an organic compound that is produced by the oxidative dehydrogenation of 3,4-dimethylaniline. It has been shown to undergo a number of reactions, including hydrochloric acid transfer hydrogenation and diazotization. This reaction yields 3-amino-4-methylbenzonitrile, dimethylamine and anilines. The transfer hydrogenation of nitroarenes with 3-amino-4-methylbenzonitrile gives 3-(3,4)-diaminobenzonitrile and 2,6-dinitrotoluene. The optimization of this reaction has led to the discovery of new nitrite derivatives as a result of the addition of nitrite in the presence of 3-amino-4-methylbenzonitrile.Formula:C8H8N2Purity:Min. 95%Color and Shape:PowderMolecular weight:132.16 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-ethynylbenzaldehydeFormula:C9H6O2Purity:Min. 95%Color and Shape:Yellow solid.Molecular weight:146.14 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/mol2,6-Dimethoxybenzaldehyde
CAS:Synthetic building block
Formula:C9H10O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:166.17 g/mol3,4-Dinitrobenzonitrile
CAS:3,4-Dinitrobenzonitrile is a fine chemical that is used as a versatile building block in the synthesis of complex organic compounds. It is also used as a research chemical and a reaction component in organic synthesis. 3,4-Dinitrobenzonitrile is stable against oxidation and hydrolysis, making it an ideal intermediate for other reactions. CAS No. 4248-33-3Formula:C7H3N3O4Purity:Min. 95%Color and Shape:PowderMolecular weight:193.12 g/mol4-Acetamidobenzoic acid
CAS:4-Acetamidobenzoic acid is an aromatic organic compound that is a precursor to many pharmaceuticals, such as acetaminophen, amoxicillin, dapsone, and sulfonamide. It is an intermediate in the formation of 4-hydroxybenzoic acid from benzoic acid. This molecule is also a component of some types of plastics. The chemical's structure and properties are determined by its coordination geometry, which consists of four nitrogen atoms and one hydroxyl group. 4-Acetamidobenzoic acid has been shown to inhibit the growth of certain bacteria by interfering with their metabolic activity. It has also been found to be active against several infectious diseases such as malaria and tuberculosis. The mechanism behind its effectiveness may be due to the fact that it inhibits bacterial fatty acid synthesis or prevents the production of ATP in mitochondria cells.br>br> br>br> The reaction solution was heated for 20 minutes at 100Formula:C9H9NO3Color and Shape:White PowderMolecular weight:179.17 g/mol3-Hydroxy-4-methylbenzaldehyde
CAS:3-Hydroxy-4-methylbenzaldehyde is a chemical that is synthesized from 3-hydroxy-4-methylphenol and dimethylformamide. It has been shown to interact with aluminium, which may be due to its ability to form a 1:1 complex with the metal. 3-Hydroxy-4-methylbenzaldehyde also exhibits electrochemical methods and isomers with other aldehydes. This chemical can be used in gas chromatography/mass spectrometry (GCMS) as an internal standard for fatty acid analysis.Formula:C8H8O2Purity:Min. 95%Color and Shape:White PowderMolecular weight:136.15 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.
Formula:C8H4ClF3O2Purity:Min. 95%Color and Shape:PowderMolecular weight:224.56 g/mol
