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(5,431 products)
- Benzyl alcohols(1,453 products)
- Halogenated Benzenes(33,758 products)
- Phenols(2,644 products)
Found 11830 products of "Benzenes"
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3,5-Dichloro-4-hydroxybenzonitrile
CAS:Formula:C7H3Cl2NOPurity:98%Color and Shape:SolidMolecular weight:188.015-Bromo-2-(bromomethyl)benzonitrile
CAS:Formula:C8H5Br2NPurity:95%Color and Shape:SolidMolecular weight:274.9433,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
CAS:Purity:≥95%Molecular weight:257.14001465-Amino-2,3-difluorobenzonitrile
CAS:Formula:C7H4F2N2Purity:97%Color and Shape:SolidMolecular weight:154.122-Hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
CAS:Purity:95%Molecular weight:245.08999632-Amino-3-nitrobenzoic acid methyl ester
CAS:Formula:C8H8N2O4Purity:98%Color and Shape:Solid, Yellow powderMolecular weight:196.1623-Methyl-4-nitrobenzonitrile
CAS:Formula:C8H6N2O2Purity:97%Color and Shape:Orange powderMolecular weight:162.1482-Cyano-5-(trifluoromethyl)phenylboronic acid
CAS:Purity:98%Color and Shape:SolidMolecular weight:214.94000242-Fluoro-4-methylbenzonitirile
CAS:Formula:C8H6FNPurity:97%Color and Shape:SolidMolecular weight:135.1414-Fluoro-2-nitrobenzonitrile
CAS:Formula:C7H3FN2O2Purity:97.0%Color and Shape:SolidMolecular weight:166.111(R)-1-(2-Nitrophenyl)pyrrolidin-3-aminehydrochloride
CAS:Formula:C10H14ClN3O2Purity:95.0%Molecular weight:243.692-Amino-5-bromo-6-fluoro-3-iodobenzonitrile
CAS:Formula:C7H3BrFIN2Purity:95.0%Molecular weight:340.9223-Fluoro-4-(piperazin-1-yl)benzonitrile
CAS:Formula:C11H12FN3Purity:98%Color and Shape:SolidMolecular weight:205.2363′-cyano-2-(4-methylpiperazinomethyl) benzophenone
CAS:Formula:C20H21N3OPurity:97.0%Molecular weight:319.4084-NITROPHENYL 3-ETHYL-4-METHYL-2-OXO-2,5-DIHYDRO-1H-PYRROLE-1-CARBOXYLATE
CAS:Formula:C14H14N2O5Purity:95.0%Molecular weight:290.2752-Fluoro-6-nitrobenzonitrile
CAS:Formula:C7H3FN2O2Purity:95%Color and Shape:SolidMolecular weight:166.1114-Chloro-3-fluoronitrobenzene
CAS:Formula:C6H3ClFNO2Purity:95%Color and Shape:SolidMolecular weight:175.543′-cyano-3-(4-thiomethylphenyl)propiophenone
CAS:Formula:C17H15NOSPurity:97.0%Molecular weight:281.372-Methyl-5-nitrophenylboronic acid
CAS:Formula:C7H8BNO4Purity:98%Color and Shape:Liquid, No data available.Molecular weight:180.954-Amino-3-nitrobenzaldehyde
CAS:Formula:C7H6N2O3Purity:96%Color and Shape:SolidMolecular weight:166.1364-ACETYL-2-METHYLBENZONITRILE
CAS:Formula:C10H9NOPurity:98%Color and Shape:SolidMolecular weight:159.188(2-BROMO-6-NITROPHENOXY)(TERT-BUTYL)DIMETHYLSILANE
CAS:Formula:C12H18BrNO3SiPurity:95.0%Molecular weight:332.269(2E)-1-(4-methoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one
CAS:Formula:C16H13NO4Purity:95.0%Molecular weight:283.2833-Nitroaniline-4-sulfonic acid
CAS:Formula:C6H6N2O5SPurity:94.0%Color and Shape:SolidMolecular weight:218.184-Methoxy-3-nitrophenylboronic acid
CAS:Formula:C7H8BNO5Purity:97%Color and Shape:SolidMolecular weight:196.951,2-Dimethyl-4-nitrobenzene
CAS:Formula:C8H9NO2Purity:95.0%Color and Shape:Solid, Light yellow crystallineMolecular weight:151.1654-Bromo-5-nitroveratrole
CAS:Formula:C8H8BrNO4Purity:98%Color and Shape:Light yellow powderMolecular weight:262.059Ref: 10-F038554
1g271.00€5g735.00€10g1,072.00€25g2,500.00€100g9,996.00€2.5g497.00€100mg82.00€250mg107.00€500mg190.00€4-Ethoxycarbonyl-2-nitrophenylboronic acid
CAS:Formula:C9H10BNO6Purity:97%Color and Shape:SolidMolecular weight:238.994-Fluoro-3-nitro-benzyl alcohol
CAS:Formula:C7H6FNO3Purity:97%Color and Shape:SolidMolecular weight:171.1272-Chloro-6-formylbenzonitrile
CAS:Formula:C8H4ClNOPurity:97%Color and Shape:SolidMolecular weight:165.58tert-Butyl 4-[(4-fluoro-2-nitrophenylamino)methyl]piperidine-1-carboxylate
CAS:Formula:C17H24FN3O4Purity:95.0%Molecular weight:353.394(R)-tert-Butyl 3-(4-nitrophenoxy)pyrrolidine-1-carboxylate
CAS:Formula:C15H20N2O5Purity:95.0%Molecular weight:308.3344-Amino-2,3-difluoro-5-nitrobenzoic acid
CAS:Formula:C7H4F2N2O4Purity:95%Color and Shape:SolidMolecular weight:218.116N-Methyl-3-nitrobenzamide
CAS:Formula:C8H8N2O3Purity:98%Color and Shape:SolidMolecular weight:180.1634-[(2-Fluoro-4-nitrophenoxy)methyl]piperidine hydrochloride
CAS:Formula:C12H16ClFN2O3Purity:95.0%Molecular weight:290.72Ethyl 1-(2-nitrophenyl)piperidine-4-carboxylate
CAS:Formula:C14H18N2O4Purity:95.0%Molecular weight:278.3085-Chloro-4-fluoro-2-methylnitrobenzene
CAS:Formula:C7H5ClFNO2Purity:98%Color and Shape:SolidMolecular weight:189.574-Chloro-3,5-dinitrobenzotrifluoride
CAS:Formula:C7H2ClF3N2O4Purity:95.0%Color and Shape:Solid, CrystallineMolecular weight:270.553-Fluoro-2-nitro-N-(piperidin-4-ylmethyl)aniline hydrochloride
CAS:Formula:C12H17ClFN3O2Purity:95.0%Molecular weight:289.74N-(2-hydroxy-5-nitrophenyl)acetamide
CAS:Formula:C8H8N2O4Color and Shape:SolidMolecular weight:196.1622-Nitro-4-methoxybenzoic acid
CAS:Formula:C8H7NO5Purity:96%Color and Shape:SolidMolecular weight:197.1463-Chloro-1-(4-nitrophenyl)-5,6-dihydropyridin-2(1H)-one
CAS:Formula:C11H9ClN2O3Purity:98%Molecular weight:252.65(2-formyl-6-methoxy-4-nitrophenoxy)acetic acid
CAS:Formula:C10H9NO7Purity:95.0%Molecular weight:255.1824-Chloro-2-nitrophenylacetic acid
CAS:Formula:C8H6ClNO4Purity:95%Color and Shape:SolidMolecular weight:215.59(S)-1-(2-Nitrophenyl)pyrrolidin-3-aminehydrochloride
CAS:Formula:C10H14ClN3O2Purity:95.0%Molecular weight:243.691-[4-Benzenesulfonyl-2-(3-nitro-phenyl)-oxazol-5-yl]-piperidine
CAS:Formula:C20H19N3O5SMolecular weight:413.452-Nitro-4-trifluoromethyl-benzoyl chloride
CAS:Formula:C8H3ClF3NO3Purity:97%Color and Shape:SolidMolecular weight:253.561-(2-chloro-4-nitrophenyl)pyrrolidine
CAS:Formula:C10H11ClN2O2Purity:97.0%Color and Shape:SolidMolecular weight:226.662-chloro-N-methoxy-N-methyl-5-nitrobenzamide
CAS:Formula:C9H9ClN2O4Purity:95.0%Molecular weight:244.63METHYL 4-AMINO-2-NITROBENZOATE
CAS:Formula:C8H8N2O4Purity:98%Color and Shape:SolidMolecular weight:196.162N-(4-Methoxy-2-methyl-6-nitrophenyl)acetamide
CAS:Formula:C10H12N2O4Purity:98%+;RGColor and Shape:No data available.Molecular weight:224.2162-[(2-Fluoro-4-nitrophenoxy)methyl]tetrahydrofuran
CAS:Formula:C11H12FNO4Purity:95.0%Molecular weight:241.218(2E)-3-(3-methoxyphenyl)-1-(3-nitrophenyl)prop-2-en-1-one
CAS:Formula:C16H13NO4Purity:95.0%Molecular weight:283.2831,5-Difluoro-2,4-dinitrobenzene
CAS:Formula:C6H2F2N2O4Purity:95.0%Color and Shape:SolidMolecular weight:204.089(R)-1-(4-Fluoro-2-nitrophenyl)pyrrolidin-3-amine hydrochloride
CAS:Formula:C10H13ClFN3O2Purity:95.0%Molecular weight:261.681-(2-Chloro-4-nitrophenyl)-4-methylpiperazine
CAS:Formula:C11H14ClN3O2Purity:95%Molecular weight:255.7N-(3-acetylphenyl)-4-methyl-3-nitrobenzamide
CAS:Formula:C16H14N2O4Purity:95.0%Molecular weight:298.2981-(4-Fluoro-2-nitrophenyl)piperidine-3-carboxylic acid
CAS:Formula:C12H13FN2O4Molecular weight:268.244METHYL 4-FLUORO-2-METHOXYMETHYL-5-NITROBENZOATE
CAS:Formula:C10H10FNO5Purity:97.0%Color and Shape:SolidMolecular weight:243.192-(4-Nitro-benzylsulfanyl)-ethylamine; hydrochloride
Formula:C9H13ClN2O2SPurity:95.0%Molecular weight:248.733-Methyl-4-nitrobenzyl bromide
CAS:Formula:C8H8BrNO2Purity:97%Color and Shape:SolidMolecular weight:230.0611-(4-Nitrophenyl)cyclopropanecarboxylic acid
CAS:Formula:C10H9NO4Purity:98%Color and Shape:SolidMolecular weight:207.185Methyl 4-[(3-methoxy-3-oxopropyl)sulfanyl]-3-nitrobenzoate
CAS:Purity:97+%Molecular weight:299.2999878Boc-His(Dnp)-OH.IPA
CAS:<p>M03289 - Boc-His(Dnp)-OH.IPA</p>Formula:C17H19N5O8Purity:98%Color and Shape:Solid, Light yellow powderMolecular weight:421.3661-Bromo-2-fluoro-4-methoxy-5-nitrobenzene
CAS:Formula:C7H5BrFNO3Purity:97%Color and Shape:Liquid, No data available.Molecular weight:250.0232-(5-BROMO-2-NITROPHENOXY)-N,N-DIMETHYLETHANAMINE
CAS:Formula:C10H13BrN2O3Purity:95.0%Molecular weight:289.1292,5-Dichloro-4-nitrophenol
CAS:Formula:C6H3Cl2NO3Purity:98%Color and Shape:SolidMolecular weight:207.994-iso-Propylamino-3-nitrobenzotrifluoride
CAS:Formula:C10H11F3N2O2Purity:97.0%Color and Shape:SolidMolecular weight:248.2054,4′-(Propane-1,3-diylbis(oxy))bis(5-methoxy-2-nitrobenzoic acid)
CAS:Purity:95%Molecular weight:466.3550112-(3-Nitrophenyl)ethanamine hydrochloride
CAS:Formula:C8H11ClN2O2Purity:95.0%Color and Shape:SolidMolecular weight:202.64(R)-tert-Butyl (1-(2-nitrophenyl)ethyl)carbamate
CAS:Formula:C13H18N2O4Purity:95.0%Molecular weight:266.2972-Amino-5-bromo-3-chlorobenzonitrile
CAS:Formula:C7H4BrClN2Purity:98%Color and Shape:SolidMolecular weight:231.483-Chloro-2-nitrobenzotrifluoride
CAS:Formula:C7H3ClF3NO2Purity:98.0%Color and Shape:Solid, Low Melting SolidMolecular weight:225.551-(3-(benzyloxy)-2-fluoro-6-nitrophenyl)propan-2-one
CAS:Formula:C16H14FNO4Purity:95.0%Molecular weight:303.289(S)-2-Amino-5-guanidino-N-(4-nitrophenyl)pentanamide dihydrochloride
CAS:Purity:97%Molecular weight:367.23Methyl 4-amino-2-methyl-5-nitrobenzoate
CAS:Formula:C9H10N2O4Purity:95%Color and Shape:SolidMolecular weight:210.189Methyl 3-bromo-5-cyanobenzoate
CAS:Formula:C9H6BrNO2Purity:95.0%Color and Shape:SolidMolecular weight:240.0562-(5-Bromo-pyrimidin-2-yloxy)-benzonitrile
CAS:Formula:C11H6BrN3OPurity:97.0%Molecular weight:276.0934-Chloro-3-nitrocinnamic acid
CAS:Formula:C9H6ClNO4Purity:98%Color and Shape:Solid, Yellow powderMolecular weight:227.61-(2-Nitrophenyl)-2-thiourea
CAS:Formula:C7H7N3O2SPurity:95.0%Color and Shape:SolidMolecular weight:197.214-Chloro-3-nitro-5-sulfamoylbenzoic acid
CAS:Formula:C7H5ClN2O6SPurity:98%Color and Shape:Liquid, No data available.Molecular weight:280.643-Chloro-4-nitrobenzotrifluoride
CAS:Formula:C7H3ClF3NO2Purity:98%Color and Shape:LiquidMolecular weight:225.552-Bromo-5-hydroxybenzoic acid methyl ester
CAS:<p>2-Bromo-5-hydroxybenzoic acid methyl ester (2BB) is a phenoxy activator that activates the glucokinase activator. It has been shown to have a glucose lowering effect in both animal and human studies. 2BB is orally bioavailable and has an allosteric mode of action, which means it works by binding to the allosteric site on the enzyme's active site, thereby increasing its activity. It binds to the benzamide of glucokinase, which causes an increase in glucose uptake and utilization by cells. 2BB is being studied for use as an oral treatment for type II diabetes mellitus.</p>Formula:C8H7BrO3Purity:Min. 95%Color and Shape:PowderMolecular weight:231.04 g/mol3,5-Diamino-2,4,6-triiodobenzoic acid
CAS:<p>3,5-Diamino-2,4,6-triiodobenzoic acid is a metabolite of hydrochloric acid and has been used in sample preparation for roentgenographic techniques. It is also used in the preparation of methylating agents for mass spectrometric analysis. It is hydrophilic with a methyl esterification that can be activated by amines. This chemical compound is found in human urine and has been shown to have an enhanced effect on tissues when combined with hydrochloric acid.</p>Formula:C7H5I3N2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:529.84 g/mol(3,5-Dimethoxy-4-hydroxyphenyl)acetone
CAS:<p>(3,5-Dimethoxy-4-hydroxyphenyl)acetone is a phenolic compound that is used as a calibration standard in the analysis of tannins. It has been shown to have a catalytic effect on the oxidation of oleic acid and linoleic acid in the presence of peroxides. The addition of (3,5-dimethoxy-4-hydroxyphenyl)acetone to an oil or fat emulsion at room temperature leads to an increase in the viscosity of the emulsion. This compound can be found in many plants, such as tea and coffee beans, cocoa beans, and red wine grapes.</p>Formula:C11H14O4Purity:Min. 95%Color and Shape:Orange PowderMolecular weight:210.23 g/mol2,4,6-Trimethylbenzonitrile
CAS:<p>2,4,6-Trimethylbenzonitrile (TMBN) is a reactive unsaturated ketone that reacts with phosphorus pentachloride to form the corresponding chloroform. It is used in nucleophilic substitution reactions and can be hydrolyzed by hydrochloric acid to form an n-oxide. The reaction mechanism of TMBN with phosphorus pentachloride has been studied using molecular modeling and NMR spectroscopy. TMBN can be converted into an oxide, which can react with hydrogen chloride to form the corresponding chloroform. Reaction products include the 2,4,6-trichlorobenzonitrile (TCBN), which is a carcinogen.</p>Formula:C10H11NPurity:Min. 95%Color and Shape:PowderMolecular weight:145.2 g/mol2-Cyanobenzaldehyde
CAS:<p>2-Cyanobenzaldehyde is an aldehyde that reacts with nucleophiles such as trifluoromethanesulfonic acid to form a molecule. 2-Cyanobenzaldehyde has potent inhibitory activity against the kinase glycogen synthase kinase 3 (GSK3) and can be used to treat autoimmune diseases. It also reacts with hydrochloric acid in solution to form an intermediate, which is then reacted with glycine and ATP to produce a chiral compound. The product of this reaction has been shown to be active methylene, which was synthesized by asymmetric synthesis.</p>Formula:C8H5NOPurity:Min. 95%Color and Shape:PowderMolecular weight:131.13 g/mol2-Fluoro-4-iodobenzonitrile
CAS:<p>2-fluoro-4-iodobenzonitrile is a potent inhibitor of the functions of VEGFR receptors. It inhibits the proliferation and migration of cancer cells by binding to VEGFR receptors, which are tyrosine kinases that regulate cell growth and differentiation. 2-Fluoro-4-iodobenzonitrile has been shown to inhibit angiogenesis, or the formation of new blood vessels, in vitro. This drug also has potent inhibitory activity against tumor growth in vivo. Clinical trials have shown that 2-fluoro-4-iodobenzonitrile can be used to treat various types of cancers, including breast cancer and colon cancer.</p>Formula:C7H3FINPurity:Min. 95%Color and Shape:PowderMolecular weight:247.01 g/mol4-Bromobenzaldehyde
CAS:<p>Please enquire for more information about 4-Bromobenzaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C7H5BrOMolecular weight:185.03 g/mol4-Bromo-3,5-dimethylbenzoic acid methyl ester
CAS:<p>4-Bromo-3,5-dimethylbenzoic acid methyl ester is a versatile building block that is used in the synthesis of complex compounds. 4-Bromo-3,5-dimethylbenzoic acid methyl ester is an intermediate in the synthesis of speciality chemicals and research chemicals. It is also a useful scaffold for the synthesis of high quality and useful reagents as well as reaction components.</p>Formula:C10H11BrO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:243.1 g/mol4-(Azidomethyl)benzoic acid
CAS:<p>4-(Azidomethyl)benzoic acid is a chemical compound that has been used in studies on mammalian cells, as well as in vitro assays. This molecule belongs to the class of organic compounds called heterocyclic compounds and contains a reactive functional group. 4-(Azidomethyl)benzoic acid can be synthetically made by combining the appropriate reactants, including lysine residues, in a solid-phase synthesis. The postsynthetic modification of this molecule includes its conversion to other molecules with different functional groups. 4-(Azidomethyl)benzoic acid has been shown to have anti-cancer properties against leukemia cells in vivo.</p>Formula:C8H7N3O2Purity:Min. 95%Molecular weight:177.16 g/mol4-Cyanobenzoic acid
CAS:<p>4-Cyanobenzoic acid (4CB) is a benzene derivative that inhibits the activity of tyrosinase, an enzyme involved in the production of melanin. It is synthesized by reacting 2,4-dichlorobenzoic acid with sodium hydroxide and acetone. 4CB has been shown to have a potent inhibitory effect on the enzyme, with an isolated yield of up to 83%. The compound also shows strong hydrogen bonding interactions with water molecules and coordinates in a geometry where one of its oxygen atoms is double bonded to two nitrogen atoms. This structural analysis suggests that 4 CB may bind to tyrosinase through adsorption mechanism.</p>Formula:C8H5NO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:147.13 g/mol4-Bromo-2-hydroxybenzaldehyde
CAS:<p>4-Bromo-2-hydroxybenzaldehyde is a versatile building block that can be used as a reaction component to synthesize other compounds. 4-Bromo-2-hydroxybenzaldehyde is a useful intermediate in the manufacture of pharmaceuticals, pesticides, and herbicides. This chemical also has various applications in research and industry. It is an important reagent for the production of polymers and resins, as well as being an essential raw material for the synthesis of pharmaceuticals and agrochemicals.</p>Formula:C7H5BrO2Molecular weight:201.02 g/molRef: 3D-W-201939
25gTo inquire50gTo inquire100gTo inquire250gTo inquire500gTo inquire-Unit-ggTo inquire3-Hydroxy-4-nitrobenzaldehyde
CAS:<p>3-Hydroxy-4-nitrobenzaldehyde is a ternary complex, which consists of three molecules that are bound to each other in a specific way. It has been observed in the nmr spectra and it has been proposed as a fluorescence probe for the detection of hydrogen bonds. 3-Hydroxy-4-nitrobenzaldehyde catalyzes the reaction by forming a covalent bond with the pbr322 dna, which is an important DNA molecule in bacteria. The enzyme mechanism is not fully understood, but it has been shown that it can bind to Toll-like receptor 4 (TLR4), which is an innate immune system protein. This binding event activates TLR4, leading to the inflammatory response. 3-Hydroxy-4-nitrobenzaldehyde has shown efficacy against microglia cells and animal experiments have shown that this compound may be useful for reducing pain after surgery or injury.</p>Formula:C7H5NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:167.12 g/mol4-Ethylbenzaldehyde
CAS:<p>4-Ethylbenzaldehyde is a chemical compound that belongs to the group of fatty acids. It has been shown to have biological properties, such as antiviral potency and genotoxic effects. This chemical compound also has a gas sensor property and is used as an exothermic reactant in organic synthesis reactions. 4-Ethylbenzaldehyde has been shown to inhibit the growth of bacteria, fungi, and viruses by blocking the synthesis of viral nucleic acid or inhibiting viral protein synthesis. The magnetic resonance spectroscopy (NMR) spectral data for 4-ethylbenzaldehyde show that this chemical compound contains two methyl groups, one on each side of the benzene ring, with a hydroxyl group on one end. The carbon atoms are bonded together in an alternating pattern of single and double bonds. The molecular formula for 4-ethylbenzaldehyde is C9H10O2.</p>Formula:C9H10OPurity:Min. 96.0%Color and Shape:PowderMolecular weight:134.18 g/mol2,3-Diaminobenzoic acid
CAS:<p>2,3-Diaminobenzoic acid is a benzimidazole derivative that is used in the treatment of microbial infections. It has been shown to inhibit the growth of bacteria by binding to their ribosomes and inhibiting protein synthesis. The reaction solution of 2,3-diaminobenzoic acid has fluorescence properties that can be used to detect contaminating substances. The conjugates formed with p-hydroxyphenylacetic acid are more soluble than those formed with hydroxybenzoic acid. 2,3-Diaminobenzoic acid is not very toxic and does not cause any detectable changes in enzyme activities or other biochemical parameters in short term exposure. It can be easily decomposed by sodium chloride into chlorine gas and hydrochloric acid, which are both highly reactive with water.</p>Formula:C7H8N2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:152.15 g/mol3,4-Dichlorobenzaldehyde
CAS:<p>3,4-Dichlorobenzaldehyde is a monosubstituted aromatic organic compound with inhibitory effects. 3,4-Dichlorobenzaldehyde has shown significant antifungal activity against Candida albicans and Saccharomyces cerevisiae. It also inhibits the growth of certain cancer cells in cell culture studies. 3,4-Dichlorobenzaldehyde has been found to have anti-inflammatory properties and would be effective in treating inflammatory diseases such as asthma or arthritis. This compound has been shown to have significant effects on energy metabolism and fatty acid synthesis by inhibiting enzymes that are involved in these processes. 3,4-Dichlorobenzaldehyde can also be used to treat metabolic disorders such as diabetes mellitus type II and hyperlipidemia by inhibiting enzymes that are involved in these processes.</p>Formula:C7H4Cl2OPurity:Min. 95%Color and Shape:White To Off-White SolidMolecular weight:175.01 g/mol4-Sulfophthalic acid (contains 3-sulfophthalic acid), 50% aqueous solution
CAS:<p>Please enquire for more information about 4-Sulfophthalic acid (contains 3-sulfophthalic acid), 50% aqueous solution including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C8H6O7SPurity:80%Molecular weight:246.2 g/mol2-Bromo-6-hydroxybenzaldehyde
CAS:<p>2-Bromo-6-hydroxybenzaldehyde is a synthetic chemical that consists of a furan ring with an acetonitrile group. It has been shown to be a constant in cyclic electroreduction and is used as a biomolecular surfactant. 2-Bromo-6-hydroxybenzaldehyde has also been shown to react intramolecularly with the hydroxyl group on the benzene ring, which results in the formation of a dimer. This chemical can be produced by solvolysis or electroreduction.</p>Formula:C7H5BrO2Purity:Min. 95%Color and Shape:PowderMolecular weight:201.02 g/mol4-(Bromomethyl) benzoic acid
CAS:<p>4-(Bromomethyl) benzoic acid (4-BA) is a chemical compound that is used as an antimicrobial agent and a reagent in organic synthesis. It has been shown to have a broad spectrum of activity against Gram-positive and Gram-negative bacteria, fungi, and protozoa. 4-BA is stable at neutral pH and can be prepared by the reaction of 2-bromobenzeneacetic acid with sodium borohydride in the presence of acetic acid. This compound reacts with nucleophiles such as imatinib, forming an iminium intermediate. The resulting product can then react with chloride or hydrogen bond to form 4-BA chloride or 4-BA hydrogen bond respectively. Magnetic resonance spectroscopy has also been used to study the magnetic properties of this compound.</p>Formula:C8H7BrO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:215.04 g/mol4-Methyl-3-nitrobenzoic acid
CAS:<p>4-Methyl-3-nitrobenzoic acid is a fine chemical that is used as a building block in the synthesis of complex compounds. It is often used as a reagent or speciality chemical, and it has a CAS number of 96-98-0. 4-Methyl-3-nitrobenzoic acid can be react with other chemicals to form useful intermediates or scaffolds for larger molecules. This chemical is versatile and can be used in many different reactions.</p>Formula:C8H7NO4Purity:Min. 98.0 Area-%Molecular weight:181.15 g/mol4-(Pyridin-2-yloxy)benzonitrile
CAS:<p>4-(Pyridin-2-yloxy)benzonitrile is a reagent that is used in the synthesis of heterocycles. It is also a useful intermediate for the preparation of highly substituted pyridine derivatives. 4-(Pyridin-2-yloxy)benzonitrile can be used to synthesize complex compounds, such as pharmaceuticals and agricultural chemicals.</p>Formula:C12H8N2OPurity:Min. 95%Molecular weight:196.2 g/mol3-(Chlorosulfonyl)benzoic acid
CAS:<p>3-(Chlorosulfonyl)benzoic acid is a synthetic compound that inhibits histone lysine methylation. It has been shown to protect against neuronal injury and cognitive impairment. 3-(Chlorosulfonyl)benzoic acid also has an inhibitory effect on the activation of Sirt2, which is an enzyme involved in cellular processes such as cancer, diabetes, inflammation, and aging. 3-(Chlorosulfonyl)benzoic acid has low potency and is not very soluble in water. It can be used to treat metabolic disorders by increasing the amount of insulin released from the pancreas and lowering blood glucose levels.</p>Formula:C7H5ClO4SPurity:Min. 95%Molecular weight:220.63 g/mol4-tert-Butylbenzaldehyde
CAS:<p>4-tert-Butylbenzaldehyde is an organic compound with the molecular formula CH3COCH2C6H5. It is a viscous liquid that is insoluble in water and has a boiling point of 146 °C. 4-tert-Butylbenzaldehyde reacts with cationic surfactants to form polymeric micelles, which are spherical structures composed of many small spherical subunits. These polymeric micelles are used as model systems for studying the properties of surfactant aggregates in solution. The reaction mechanism for this polymerization process involves the oxidation of 4-tert-butylbenzaldehyde by hydrogen peroxide and the subsequent condensation of 4-tert-butylbenzoic acid with malonic acid or other cinnamic acid derivatives to form the corresponding esters. The oxidized product, 4-tert-butylbenzoic acid, can be regenerated by boiling a mixture containing it</p>Formula:C11H14OPurity:Min. 96.5%Color and Shape:Colorless Clear LiquidMolecular weight:162.23 g/mol1,4-Dicaffeoylquinic acid
CAS:<p>1,4-Dicaffeoylquinic acid: an antioxidant and selective HIV-1 integrase inhibitor, non-toxic at effective doses.</p>Formula:C25H24O12Purity:97.32%Color and Shape:SolidMolecular weight:516.454-Hydrazinobenzoic acid
CAS:<p>4-Hydrazinobenzoic acid is a chemical compound that is used as an inhibitor of DNA synthesis. It prevents the formation of hydrogen bonds between nucleotides in DNA, which prevents the synthesis of new DNA strands. 4-Hydrazinobenzoic acid has been shown to inhibit the growth of human breast cancer cells by reactivating the tumor suppressor genes p21 and Rb1, which are responsible for regulating cell cycle progression. This compound also inhibits the production of hydrogen chloride (HCl) in reaction solutions containing sodium hypochlorite (NaOCl).</p>Formula:C7H8N2O2Purity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:152.15 g/mol4-Bromobenzaldehyde
CAS:<p>4-Bromobenzaldehyde is a chemical compound that belongs to the group of aromatic compounds. It has been shown to have a potent stimulatory effect on locomotor activity in mice, which may be due to its ability to increase levels of epidermal growth factor and gamma-aminobutyric acid in the brain. 4-Bromobenzaldehyde can be synthesized from 2,4-dibromophenol and anhydrous copper chloride in the presence of sodium hydroxide. The reaction mechanism for this synthesis is believed to involve an intermediate enamine form of 4-bromobenzaldehyde, which can then undergo hydrolysis into 2,4-dibromophenol and benzaldehyde. This product is used as a reagent in organic synthesis because it can be used to form esters with trifluoroacetic acid or hydrochloric acid in high yield.</p>Formula:C7H5BrOPurity:Min. 90 Area-%Color and Shape:White PowderMolecular weight:185.02 g/mol3-Fluoro-4-hydroxybenzonitrile
CAS:<p>3-Fluoro-4-hydroxybenzonitrile is a compound with an acidic ph and a strain that is dispersive, desorptive, and polyacrylamide gel. It is a colorless liquid at room temperature. 3-Fluoro-4-hydroxybenzonitrile has been shown to react with dodecyl inorganic base and hydrochloric acid to produce 3-fluoroaniline. The localization of the reaction yield is on hydrotalcite activated by fluorine. This chemical has been shown to react at temperatures between 0°C and 140°C.</p>Formula:C7H4FNOPurity:Min. 95%Color and Shape:White PowderMolecular weight:137.11 g/mol4-Formylbenzoic acid
CAS:<p>4-Formylbenzoic acid is an organic compound with the molecular formula CH2=C(O)CH=CHCO2H. It is a white solid that is soluble in water and has a strong, unpleasant odor. 4-Formylbenzoic acid has been shown to have affinity for binding to odorous molecules such as sulfur compounds, amines, and mercaptans. The binding of these molecules to the 4-formylbenzoic acid leads to a decrease in their odor concentration. This process can be done using electrochemical impedance spectroscopy or optical sensors. The oxidation of 4-formylbenzoic acid by trifluoroacetic acid produces 2-formylphenol and formaldehyde, which are themselves volatile compounds with an unpleasant odor. These reactions may be used as wastewater treatment methods. Langmuir adsorption isotherm may be used as an analytical method for measuring the concentration of 4-formylbenzoic acid</p>Formula:C8H6O3Purity:Min. 98 Area-%Color and Shape:White Yellow PowderMolecular weight:150.13 g/molMethyl 3,4-dimethoxybenzoate
CAS:<p>Methyl 3,4-dimethoxybenzoate is an acetate extract that has been shown to inhibit tyrosinase activity. This compound also has a potent inhibitory effect on the production of p-hydroxybenzoic acid. Methyl 3,4-dimethoxybenzoate can be synthesized from protocatechuic acid and methoxy groups. It is a chemical reaction involving three steps: condensation, dehydration, and reduction. Tyrosinase is an enzyme in the melanin biosynthetic pathway that catalyzes the conversion of tyrosine to dopaquinone. Tyrosinase activity can be inhibited by methyl 3,4-dimethoxybenzoate through competitive inhibition or by its ability to reduce the availability of substrate for this enzyme.</p>Formula:C10H12O4Purity:Min. 95%Color and Shape:PowderMolecular weight:196.2 g/mol2-Iodobenzoic acid methyl ester
CAS:<p>2-Iodobenzoic acid methyl ester is a palladium complex that can be used as a catalyst for the hydrolysis of ketoesters, imines, and halides. The reaction mechanism involves the coordination of the metal center to the carboxylate or amine group on the substrate, followed by a nucleophilic attack at the benzoate or chloride group. The resulting product is an alkyl halide. 2-Iodobenzoic acid methyl ester has been shown to catalyze the cross-coupling of diphenyl ethers with various amines in water and in organic solvents.</p>Formula:C8H7IO2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:262.04 g/mol3,5-Dimethylbenzaldehyde
CAS:<p>3,5-Dimethylbenzaldehyde is an organic compound that is a colorless liquid. It has a chemical formula of C9H12O2 and is classified as an aldehyde. 3,5-Dimethylbenzaldehyde can be synthesized by the reaction of isopropyl palmitate with xylene in the presence of carbon as a source. The reaction time required for this synthesis is approximately one day. The major products of this reaction are 3,5-dimethylbenzaldehyde and 2-methylbutanal. This reaction mechanism can also be used to determine the concentration of urinary metabolites in human urine samples. Analysis of these samples requires an organic solvent such as hexane or dichloromethane. Kinetic data was collected from the rate at which zinc powder reacts with 3,5-dimethylbenzaldehyde over time at different concentrations. A kinetic experiment was conducted using c–h bond activation to produce 3,5-dimethoxy</p>Formula:C9H10OPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:134.18 g/mol2-(Boc-aminomethyl)benzoic acid
CAS:<p>2-(Boc-aminomethyl)benzoic acid is a versatile building block with a wide range of applications in the field of organic chemistry. It has been shown to be useful as a reagent in the synthesis of complex compounds and fine chemicals, as well as a reaction component for the preparation of pharmaceuticals. 2-(Boc-aminomethyl)benzoic acid can also be used as an intermediate in the synthesis of speciality chemicals such as herbicides, pesticides, and fungicides.</p>Formula:C13H17NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:251.28 g/mol3,5-Dihydroxy-4-methylbenzoic acid
CAS:<p>3,5-Dihydroxy-4-methylbenzoic acid is an efficient synthesis of the natural product lucidin. It is a quinone that is found in citrifolia and morindone, compounds which are used as analgesics and antipyretics. This compound has been shown to inhibit the growth of fungi by inhibition of protein synthesis. 3,5-Dihydroxy-4-methylbenzoic acid also inhibits the production of citric acid cycle intermediates such as succinic acid and fumaric acid.</p>Formula:C8H8O4Purity:Min. 80%Color and Shape:PowderMolecular weight:168.15 g/mol2-Iodobenzoic acid
CAS:<p>2-Iodobenzoic acid is a synthetic compound that is used in the treatment of wastewater. It is produced by the reaction of benzoate and nitrite in the presence of sodium hydroxide. The intramolecular hydrogen atom transfer from the 2-iodobenzoic acid to benzoate is a reversible reaction. This process can be catalyzed by palladium, which has been shown to be effective in coupling 2-iodobenzoic acid with other compounds to produce cyclic peptides. The use of 2-iodobenzoic acid as a contraceptive has been investigated for its ability to inhibit acetylcholinesterase activity, which may lead to increased levels of acetylcholine and inhibition of muscle contractions.</p>Formula:C7H5IO2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:248.02 g/mol5-Iodo-2-nitrobenzoic acid
CAS:<p>5-Iodo-2-nitrobenzoic acid is a fine chemical that is used as a building block in the synthesis of complex compounds and research chemicals. This compound has been shown to be an effective reagent for the synthesis of many different types of compounds. It can also be used as a reactant or intermediate in organic syntheses, such as those involving cross-coupling reactions. 5-Iodo-2-nitrobenzoic acid is a versatile building block that can be used in both simple and complex chemical reactions.</p>Formula:C7H4INO4Purity:Min. 95%Color and Shape:Yellow PowderMolecular weight:293.02 g/molMethyl 3-bromobenzoate
CAS:<p>Methyl 3-bromobenzoate is a cross-coupled compound with three functional groups: a methyl group, an acid bromo group, and a carboxylic acid benzoic ester. It is used in the synthesis of antigens that are chemically reactive to trifluoroacetic acid gas. The clinical studies have shown that the efficiency of this study is low because it has been found to be difficult to synthesize methyl 3-bromobenzoate in large quantities. This molecule can be prepared by the reaction of vinylene with an electrophile in non-polar solvents or by catalytic mechanisms.</p>Formula:C8H7BrO2Purity:Min. 95%Color and Shape:White PowderMolecular weight:215.04 g/mol(-)-Corey lactone 4-phenylbenzoate
CAS:<p>Corey lactone 4-phenylbenzoate is an efficient, large-scale preparation of (-)-Corey lactone. It is synthesized in two steps from 4-phenylbenzoic acid and ethyl acetoacetate. Corey lactone 4-phenylbenzoate has been used for the synthesis of a variety of natural products. This compound is also a precursor to the synthesis of other compounds, such as 3-amino-4-(2'-hydroxyethoxy)benzaldehyde.</p>Formula:C21H20O5Purity:Min. 95%Molecular weight:352.38 g/mol4-tert-Butoxybenzaldehyde
CAS:<p>4-tert-Butoxybenzaldehyde is a colorless liquid that has a viscosity of 0.3 mm2/s at 25 °C. It can be synthesized by reacting pyridine with hydrochloric acid in the presence of a Grignard reagent. 4-tert-Butoxybenzaldehyde reacts with phenolic antioxidants to form an ester, which can be used as an industrial solvent. The crystal x-ray diffraction pattern of 4-tert-Butoxybenzaldehyde exhibits peaks at 2θ = 8.0, 11.5, and 18.5° corresponding to the (100), (200), and (220) planes, respectively. This chemical can also undergo reactions that lead to termination or transfer reactions, including diethyl ketomalonate formation with diethyl malonate in the presence of water as a solvent and potassium hydroxide as a catalyst for transfer reactions.END></p>Formula:C11H14O2Purity:Min. 95%Color and Shape:PowderMolecular weight:178.23 g/mol3-Chloro-5-iodobenzoic acid methyl ester
CAS:<p>3-Chloro-5-iodobenzoic acid methyl ester is a versatile building block that can be used to make many complex compounds, including research chemicals and reagents. 3-Chloro-5-iodobenzoic acid methyl ester is used as an intermediate for the production of speciality chemicals and has many uses in chemical reactions. This compound was previously sold under the CAS number 289039-85-6.</p>Formula:C8H6ClIO2Purity:Min. 95%Color and Shape:PowderMolecular weight:296.49 g/mol2-Chlorobenzonitrile
CAS:<p>2-Chlorobenzonitrile is a white solid that is soluble in organic solvents. It is an aryl halide and has a chemical structure of C6ClCN. 2-Chlorobenzonitrile is used as a raw material for the production of dyes and pharmaceuticals. This compound reacts with hydrochloric acid to form 4-chlorobenzonitrile, which can be used in the synthesis of other chemicals. 2-Chlorobenzonitrile can also react with n-dimethyl formamide in an optimal reaction solution to form 4-chlorobenzonitrile. The FTIR spectroscopy on this compound shows that it has a chloride group at 795 cm−1. The optimum reaction temperature for this compound is between 100 and 120 °C, but it will react with inorganic acids such as sulfuric acid or phosphoric acid at higher temperatures. Synthesis of this compound can be done by reacting</p>Formula:C7H4ClNPurity:Min. 95%Color and Shape:White PowderMolecular weight:137.57 g/mol4,6-Dimethoxysalicylaldehyde
CAS:<p>4,6-Dimethoxysalicylaldehyde is a protonated molecule with a cyclohexane ring and 4 hydroxyl groups. Its chemical formula is C6H8O3. The compound has low bioavailability due to the presence of an intramolecular hydrogen bond that causes high redox potential. There are two amines on the aromatic ring which can coordinate with metal ions to form a complex. This compound's structural analysis has been conducted using X-ray crystallography, NMR spectroscopy, and IR spectroscopy. The structure of 4,6-dimethoxysalicylaldehyde is unsymmetrical due to the presence of two asymmetric carbon atoms in the molecule. It forms hydrogen bonds with other molecules due to its hydroxyl group and intramolecular hydrogen bond. Hydrogen bonding interactions occur between this compound and other molecules including water, alcohols, ammonia, amines, and carboxylic acids.</p>Formula:C9H10O4Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:182.17 g/mol2,4,5-Trimethoxybenzylamine
CAS:<p>2,4,5-Trimethoxybenzylamine is a synthetic compound that can be used as a precursor to the synthesis of other chemicals. It is prepared by reacting phenol with deuterium gas in a process called amination. This reaction is followed by reductive quaternization with cyanide. 2,4,5-Trimethoxybenzylamine is often used as an intermediate for the synthesis of drugs such as tamoxifen and clonidine.</p>Formula:C10H15NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:197.23 g/mol2-Acetylbenzoic acid
CAS:<p>2-Acetylbenzoic acid is a functional molecule that contains an acetyl group. It can form hydrogen bonds with other molecules and has been shown to induce apoptosis in cells. The reaction products of 2-acetylbenzoic acid are malonic acid, acetylsalicylic acid, and 2-benzoylbenzoic acid. These three compounds are made by the addition of hydrogen or hydroxide to the molecule 2-acetylbenzoic acid. The molecule has two functional groups: a carbonyl group and an acetyl group. The chemical structure of this molecule can be seen in the figure below.<br>2-Acetylbenzoic Acid</p>Formula:C9H8O3Purity:Min. 95%Color and Shape:PowderMolecular weight:164.16 g/mol
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