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(2,646 products)
Found 11830 products of "Benzenes"
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2-Methoxy-5-nitrophenyl isothiocyanate
CAS:Formula:C8H6N2O3SPurity:98.0%Color and Shape:SolidMolecular weight:210.213-Bromo-4-chloro-5-nitrotoluene
CAS:Formula:C7H5BrClNO2Purity:≥95%Color and Shape:Solid, No data available.Molecular weight:250.485-Hydroxy-4-methoxy-2-nitrobenzoic acid
CAS:Formula:C8H7NO6Purity:96%Color and Shape:SolidMolecular weight:213.1452-(4-Chloro-3-nitrobenzoyl)benzoic acid
CAS:Formula:C14H8ClNO5Purity:≥97%Color and Shape:SolidMolecular weight:305.67Methyl 2-(2-nitro-4-(trifluoromethyl)phenyl)acetate
CAS:Formula:C10H8F3NO4Purity:95.0%Color and Shape:SolidMolecular weight:263.172N-(4,5-Dichloro-2-nitrophenyl)acetamide
CAS:Formula:C8H6Cl2N2O3Purity:97%Color and Shape:SolidMolecular weight:249.051-Methoxy-3-nitrobenzene
CAS:Formula:C7H7NO3Purity:95.0%Color and Shape:SolidMolecular weight:153.1374-(3,5-dinitrobenzoyl)-1-oxa-4-azaspiro[4.5]decane-3-carboxylic acid
CAS:Formula:C16H17N3O8Purity:95.0%Molecular weight:379.3252,5-Dibromo-4-fluoronitrobenzene
CAS:Formula:C6H2Br2FNO2Purity:97%Color and Shape:SolidMolecular weight:298.893(2E)-1-(3-methoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one
CAS:Formula:C16H13NO4Purity:95.0%Molecular weight:283.2832-BUTYRAMIDO-3-NITROPHENYL TRIFLUOROMETHANESULFONATE
CAS:Formula:C11H11F3N2O6SPurity:95.0%Molecular weight:356.272,6-Dimethyl-3-nitroaniline
CAS:Formula:C8H10N2O2Purity:98%Color and Shape:Pale-yellow to yellow-brown solidMolecular weight:166.184-Nitrobenzene-1,2-diamine hydrochloride
CAS:Formula:C6H8ClN3O2Purity:99%(LC-MS);RGMolecular weight:189.6(R)-3-(4-Fluoro-2-nitrophenoxy)pyrrolidine hydrochloride
CAS:Formula:C10H12ClFN2O3Purity:95.0%Molecular weight:262.671-(5-(2-Methyl-1H-imidazol-1-yl)-2-nitrophenyl)piperazine dihydrochloride
CAS:Formula:C14H19Cl2N5O2Molecular weight:360.24N-(4-Bromo-2-nitrophenyl)-2-chloroacetamide
CAS:Formula:C8H6BrClN2O3Purity:95.0%Molecular weight:293.53-(4-Nitrophenyl)acrylic acid
CAS:Formula:C9H7NO4Purity:95.0%Color and Shape:Crystalline PowderMolecular weight:193.158Boc-4-Nitro-D-phenylalanine
CAS:<p>M03220 - Boc-4-Nitro-D-phenylalanine</p>Formula:C14H18N2O6Purity:96%Color and Shape:Solid, White powderMolecular weight:310.3064-Fluoro-1-(3-methoxypropoxy)-2-nitrobenzene
CAS:Formula:C10H12FNO4Purity:95.0%Molecular weight:229.2072-((2-Amino-4-nitrophenyl)amino)ethanol
CAS:Formula:C8H11N3O3Purity:95.0%Color and Shape:SolidMolecular weight:197.194(2E)-1-(4-nitrophenyl)-3-[4-(propan-2-yl)phenyl]prop-2-en-1-one
CAS:Formula:C18H17NO3Purity:95.0%Molecular weight:295.338O-(4-Nitro-2-(trifluoromethyl)phenyl)hydroxylamine
CAS:Formula:C7H5F3N2O3Purity:97%Molecular weight:222.1233,5-Dichloro-2-nitroaniline
CAS:Formula:C6H4Cl2N2O2Purity:97%Color and Shape:Solid, No data available.Molecular weight:207.014-[(4-Fluoro-2-nitrophenoxy)methyl]piperidine hydrochloride
CAS:Formula:C12H16ClFN2O3Purity:95.0%Molecular weight:290.72(2E)-1-(4-nitrophenyl)-3-(2,3,4-trimethoxyphenyl)prop-2-en-1-one
CAS:Formula:C18H17NO6Purity:95.0%Molecular weight:343.335(R)-tert-Butyl 3-(2-fluoro-6-nitrophenoxy)pyrrolidine-1-carboxylate
CAS:Formula:C15H19FN2O5Purity:95.0%Molecular weight:326.3243-Amino-3-(4-fluoro-3-nitrophenyl)propanoic acid
CAS:Formula:C9H9FN2O4Purity:95.0%Molecular weight:228.1792,5-Di-tert-butylnitrobenzene
CAS:Formula:C14H21NO2Color and Shape:No data available.Molecular weight:235.3272-Chloro-4-nitrobenzenesulfonyl chloride
CAS:Formula:C6H3Cl2NO4SPurity:95%Color and Shape:SolidMolecular weight:256.054-Iodo-2-nitrobenzoic acid
CAS:Formula:C7H4INO4Purity:97.0%Color and Shape:SolidMolecular weight:293.016N1-(4-Methyl-2-nitrophenyl)propane-1,3-diamine hydrochloride
CAS:Formula:C10H16ClN3O2Purity:97.0%Molecular weight:245.713-Bromo-2-iodo-5-methoxynitrobenzene
CAS:Formula:C7H5BrINO3Purity:95.0%Color and Shape:SolidMolecular weight:357.929(R)-1-(2-Fluoro-6-nitrophenyl)pyrrolidin-3-amine hydrochloride
CAS:Formula:C10H13ClFN3O2Purity:95.0%Molecular weight:261.68n-(Tert-butyl)-2-nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CAS:Purity:95%Molecular weight:320.2000122(R)-5-(Methoxycarbonyl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylic acid
CAS:Formula:C16H16N2O6Purity:97%Molecular weight:332.312(2-Morpholin-4-yl-5-nitro-phenyl)-methanol
CAS:Formula:C11H14N2O4Purity:95.0%Molecular weight:238.2431-(3-Nitrophenyl)-3-(piperidin-4-yl)ureahydrochloride
CAS:Formula:C12H17ClN4O3Purity:95.0%Molecular weight:300.741,4-Dichloro-2-nitrobenzene
CAS:Formula:C6H3Cl2NO2Purity:99.0%Color and Shape:SolidMolecular weight:1924-Nitrophenyl hexanoate
CAS:Formula:C12H15NO4Purity:95%Color and Shape:Liquid, No data available.Molecular weight:237.2555-Amino-3-methyl-1-(3-nitrophenyl)-1H-pyrazole-4-carbonitrile
CAS:Formula:C11H9N5O2Purity:95.0%Molecular weight:243.2265-chloro-3-[(4-nitrophenyl)methyl]-1,2,4-thiadiazole
CAS:Formula:C9H6ClN3O2SPurity:95.0%Molecular weight:255.683,5-Dinitrobenzotrifluoride
CAS:Formula:C7H3F3N2O4Purity:99.0%Color and Shape:SolidMolecular weight:236.1062-Methoxy-5-nitroaniline hydrochloride
CAS:Formula:C7H9ClN2O3Purity:98%+;RGColor and Shape:SolidMolecular weight:204.61(2-CHLORO-4-NITROPHENYL)(PIPERAZIN-1-YL)METHANONE HCL
CAS:Formula:C11H13Cl2N3O3Purity:95.0%Molecular weight:306.14Ethyl 2-(4-nitrophenyl)-3-(trifluoromethyl)-pyrazole-4-carboxylate
CAS:Formula:C13H10F3N3O4Purity:97%(GC-MS);RGMolecular weight:329.235N-[2-Nitro-4-(trifluoromethyl)phenyl]piperidine
CAS:Formula:C12H13F3N2O2Purity:95.0%Molecular weight:274.243(4-Nitro-phenyl)-piperazin-1-yl-methanone
CAS:Formula:C11H13N3O3Purity:98%Color and Shape:SolidMolecular weight:235.2433-Bromo-N-methoxy-N-methyl-5-nitrobenzamide
CAS:Formula:C9H9BrN2O4Purity:97.0%Molecular weight:289.085(S)-tert-Butyl 1-(3-fluoro-2-nitrophenyl)pyrrolidin-3-ylcarbamate
CAS:Formula:C15H20FN3O4Purity:95.0%Molecular weight:325.34N,N-Dimethyl-2-nitro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
CAS:Purity:95%Molecular weight:292.14001461-([4-Nitro-3-(trifluoromethyl)phenyl]piperidine)-3-carboxylic acid
CAS:Formula:C13H13F3N2O4Molecular weight:318.252tert-Butyl 1-(2-nitrobenzoyl)piperidin-4-ylcarbamate
CAS:Formula:C17H23N3O5Purity:95.0%Molecular weight:349.387Ethyl 4-amino-2-nitrobenzoate
CAS:Formula:C9H10N2O4Purity:95%+(LC-MS);RGColor and Shape:SolidMolecular weight:210.189(3-Nitrophenyl)methanamine
CAS:Formula:C7H8N2O2Purity:95.0%Color and Shape:OilMolecular weight:152.1534-Chloro-2-nitrophenylsulfonylchloride
CAS:Formula:C6H3Cl2NO4SPurity:97%Color and Shape:SolidMolecular weight:256.05(5E)-5-(2-chloro-5-nitrobenzylidene)-1,3-thiazolidine-2,4-dione
CAS:Formula:C10H5ClN2O4SPurity:95.0%Molecular weight:284.672-Chloro-5-nitrophenyl isothiocyanate
CAS:Formula:C7H3ClN2O2SPurity:97.0%Color and Shape:SolidMolecular weight:214.621-(Difluoromethyl)-2-nitrobenzene
CAS:Formula:C7H5F2NO2Purity:95%Color and Shape:Solid, Low Melting SolidMolecular weight:173.1194-Nitrophenyl trifluoroacetate
CAS:Formula:C8H4F3NO4Purity:95%Color and Shape:SolidMolecular weight:235.1185-(2-Methyl-1H-imidazol-1-yl)-2-nitrobenzoic acid
CAS:Formula:C11H9N3O4Purity:95%Molecular weight:247.21(2E)-3-(3-nitrophenyl)-1-phenylprop-2-en-1-one
Formula:C15H11NO3Purity:98%(GC-MS);RGMolecular weight:253.2572-Amino-6-chloro-4-nitrophenol
CAS:Formula:C6H5ClN2O3Purity:97%Color and Shape:Solid, Reddish yellow - Deep yellow red powderMolecular weight:188.57METHYL 5-METHYL-2-NITROBENZOATE
CAS:Formula:C9H9NO4Purity:98%Color and Shape:Solid, White - Very pale yellow powderMolecular weight:195.1746-FLUORO-2-METHYL-3-NITROBENZOIC ACID
CAS:Formula:C8H6FNO4Purity:98%Color and Shape:SolidMolecular weight:199.137Methyl 4-(4-(1-aminoethyl)-2-methoxy-5-nitrophenoxy)butanoate hydrochloride
CAS:Purity:97%Molecular weight:348.77999883′-Amino-biphenyl-4-carbonitrile
CAS:Formula:C13H10N2Purity:97%Color and Shape:SolidMolecular weight:194.237N-(4-Chlorophenyl)-2-nitroaniline
CAS:Formula:C12H9ClN2O2Purity:97%Color and Shape:Solid, Low Melting SolidMolecular weight:248.67N-(2-methoxy-4-nitrophenyl)-3-oxobutanamide
CAS:Formula:C11H12N2O5Purity:95.0%Molecular weight:252.226N-(3-acetylphenyl)-4-methyl-3-nitrobenzamide
CAS:Formula:C16H14N2O4Purity:95.0%Molecular weight:298.2983-methoxy-4-[(2-nitrobenzyl)oxy]benzaldehyde
CAS:Formula:C15H13NO5Purity:95.0%Molecular weight:287.271Methyl 4-[(3-methoxy-3-oxopropyl)sulfanyl]-3-nitrobenzoate
CAS:Purity:97+%Molecular weight:299.29998782-(5-BROMO-2-NITROPHENOXY)-N,N-DIMETHYLETHANAMINE
CAS:Formula:C10H13BrN2O3Purity:95.0%Molecular weight:289.1294,4′-(Propane-1,3-diylbis(oxy))bis(5-methoxy-2-nitrobenzoic acid)
CAS:Purity:95%Molecular weight:466.355011METHYL 4-[4-(HYDROXYMETHYL)-2-METHOXY-5-NITROPHENOXY]BUTANOATE
CAS:Purity:98%Molecular weight:299.2789917N-Methyl-N-[4-(methylsulfonyl)-2-nitrophenyl]amine
CAS:Formula:C8H10N2O4SPurity:95.0%Color and Shape:SolidMolecular weight:230.242-(2-formyl-6-methoxy-4-nitrophenoxy)propanoic acid
CAS:Formula:C11H11NO7Purity:95.0%Molecular weight:269.2092-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/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/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-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 inquire4-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-(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/mol3-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/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/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/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/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/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/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/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/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/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/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/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/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/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/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/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/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:516.452-(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/molMethyl 4-amino-2-methoxybenzoate
CAS:<p>Methyl 4-amino-2-methoxybenzoate is a solute with anticancer activity. It has been shown to inhibit the growth of erythrocytes and cancer cells in vitro. The mechanism of action is associated with its ability to bind to aminobenzothiazole, which inhibits the production of DNA and RNA. Methyl 4-amino-2-methoxybenzoate has also been shown to inhibit the proliferation of human muscle cells and induce their differentiation. This drug does not have any effect on lipid or protein synthesis in cells, which may be due to its solvent perturbation properties.</p>Formula:C9H11NO3Purity:Min. 95%Color and Shape:PowderMolecular weight:181.19 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-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/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/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/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/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/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/mol2-Methyl-5-nitrobenzaldehyde
CAS:<p>2-Methyl-5-nitrobenzaldehyde is a nitro compound that is used in the synthesis of dobutamine. It has been shown to undergo rearrangements, with the formation of 2-methyl-5-nitrophenol. Kinetic studies have shown that chlorine can be substituted for hydrogen at the 2 position, and this substitution leads to an increase in reactivity. 2-methyl-5-nitrobenzaldehyde also reacts with dopamine to form a ketone. The hydroxy group on this molecule is nucleophilic and can attack electrophiles, making it useful as an active site for synthetic reactions. This compound is also pyrophoric, which means it will spontaneously ignite in air and burn until all its fuel is consumed.</p>Formula:C8H7NO3Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:165.15 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/mol4-Hydrazinobenzoic acid hydrochloride
CAS:<p>4-Hydrazinobenzoic acid hydrochloride is a chemical species that has an oxidative effect on DNA. It is a reactive oxygen species (ROS) that changes the hydrogen spectrum of water. The hydrogen bond is broken and the electrons in the molecule are excited to a higher energy level, which results in ROS formation. 4-Hydrazinobenzoic acid hydrochloride also inhibits mitochondrial function and causes heart disease by increasing blood pressure and weakening the heart muscle. This compound can be used as a cancer treatment for human cells, because it suppresses genes that promote cell growth. In addition, 4-hydrazinobenzoic acid hydrochloride may inhibit endothelial cell proliferation in animal experiments.</p>Formula:C7H8N2O2•HClPurity:Min. 95%Color and Shape:PowderMolecular weight:188.61 g/mol4-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/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/mol2,4,5-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/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 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/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/mol1-Cyano-4-(dimethylamino)benzene
CAS:<p>1-Cyano-4-(dimethylamino)benzene is a molecule that has been shown to inhibit the growth of hamster v79 cells. It also inhibits the synthesis of DNA and RNA. The binding constants for this molecule have been determined to be 1.0 x 10^9 M^-1, with an n-octanol/water partition coefficient (log P) of 5.5. This molecule is soluble in nonpolar solvents and may be used as a model system for hydrogen bonding interactions or reaction mechanisms in organic chemistry. This compound contains a deuterium isotope and can be used to study the effects of hydrogen bonding on reactions in organic chemistry at high temperatures, with the use of preparative hplc.</p>Formula:C9H10N2Purity:Min. 95%Color and Shape:Beige PowderMolecular weight:146.19 g/mol
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