Bencenos
Los bencenos son hidrocarburos aromáticos simples que consisten en un anillo de carbono de seis miembros con dobles enlaces alternados. Esta estructura fundamental es un bloque de construcción para numerosos compuestos químicos, incluidos productos farmacéuticos, polímeros y colorantes. Los bencenos se utilizan ampliamente en la síntesis orgánica debido a su estabilidad y versatilidad. En CymitQuimica, ofrecemos una amplia gama de bencenos de alta calidad para apoyar sus investigaciones y aplicaciones industriales.
Subcategorías de "Bencenos"
- Benzamidas(62 productos)
- Ácidos benzoicos(5.475 productos)
- Alcoholes bencílicos(1.458 productos)
- Bencenos halogenados(33.965 productos)
- Fenoles(2.663 productos)
Se han encontrado 11888 productos de "Bencenos"
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3,4-Dihydroxy-5-methoxybenzaldehyde
CAS:3,4-Dihydroxy-5-methoxybenzaldehyde is a synthetic compound that has shown to have inhibitory effects on the replication of DNA and RNA. It also inhibits the growth of bacteria in culture by binding to the nucleic acid. The chemical structure of 3,4-Dihydroxy-5-methoxybenzaldehyde is similar to that of bisbenzylisoquinoline alkaloids, which are found in plants such as opium poppy. This similarity may explain its ability to inhibit bacterial growth. 3,4-Dihydroxy-5-methoxybenzaldehyde may be used as a drug candidate for treating bacterial infections.Fórmula:C8H8O4Pureza:Min. 95%Forma y color:PowderPeso molecular:168.15 g/mol3-Amino-2-hydroxybenzoic acid
CAS:3-Amino-2-hydroxybenzoic acid (AAHB) is a nonsteroidal anti-inflammatory drug that belongs to the group of pharmaceutical preparations. It inhibits the enzyme dehydroascorbate reductase, which is involved in the production of hydrogen peroxide and other reactive oxygen species by phagocytes. Hydrogen peroxide and other reactive oxygen species can cause DNA damage and lead to cancer development. AAHB may also have antimicrobial effects, as it has been shown to inhibit bacterial growth and cell adhesion. AAHB interacts with fatty acids in a similar manner as aspirin does, but with a lower potency. It has been shown to inhibit prostaglandin synthesis by inhibiting lipoxygenase activity. The binding of AAHB at these sites prevents the formation of arachidonic acid from linoleic acid and blocks the conversion of arachidonic acid into prostaglandin H2 (PGH2).Fórmula:C7H7NO3Pureza:Min. 98 Area-%Forma y color:Off-White PowderPeso molecular:153.14 g/mol5-Acetyl-2-aminobenzonitrile
CAS:5-Acetyl-2-aminobenzonitrile is a versatile building block that can be used as an intermediate in the synthesis of a wide range of chemicals. It has been used to produce pharmaceuticals and other useful compounds, including research chemicals and speciality chemicals. 5-Acetyl-2-aminobenzonitrile is also a useful reagent for the production of organic products. The compound is available at high purity levels.
Fórmula:C9H8N2OPureza:Min. 95%Forma y color:White PowderPeso molecular:160.17 g/molMethyl 5-chlorosalicylate
CAS:Methyl 5-chlorosalicylate is a chemical compound with the molecular formula CHClO. It is a colorless liquid that has a minty odor. Methyl 5-chlorosalicylate is used in organic chemistry as an intermediate to synthesize other compounds, and it can be used in the synthesis of β-cell receptor antagonists. This drug is an analog of salicylic acid and its anti-inflammatory effects are due to the inhibition of chloride channels on macrophages. The drug's neutralizing properties have been shown by experiments with neutralizing antibody levels at physiological levels, which blocks viral replication and prevents cell damage by free radicals.Fórmula:C8H7ClO3Pureza:Min. 95%Forma y color:White PowderPeso molecular:186.59 g/molMethyl 4-amino-2-methyl benzoate
CAS:Methyl 4-amino-2-methyl benzoate is a fine chemical that can be used as a building block for research chemicals, pharmaceuticals, and speciality chemicals. Methyl 4-amino-2-methyl benzoate is a versatile building block in organic synthesis because it can be used as a reaction component and intermediate to synthesize other compounds. This compound is also an excellent scaffold for the synthesis of complex compounds, making it a useful intermediate for organic chemistry. Methyl 4-amino-2-methyl benzoate has CAS No. 6933-47-7 and is soluble in organic solvents such as dichloromethane, chloroform, ether, or acetone.Fórmula:C9H11NO2Pureza:Min. 95%Forma y color:PowderPeso molecular:165.19 g/mol3-Cyanobenzoic acid
CAS:3-Cyanobenzoic acid is a chemical intermediate that is used to synthesize 3-cyanobenzamide. It is also a byproduct of the synthesis of benzonitrile and can be found in metal surface residues and environmental pollution. The molecule has two functional groups, one electron withdrawing and one electron donating, which are necessary for its stability. This compound can be found in high concentrations when it reacts with metal surfaces or organic solvents. 3-Cyanobenzamide was synthesized from 3-cyanobenzoic acid as an amide, which has been shown to have antimicrobial properties against Gram-positive bacteria such as Staphylococcus aureus, Streptococcus pyogenes and Enterococcus faecalis.Fórmula:C8H5O2NPureza:Min. 95%Forma y color:PowderPeso molecular:147.13 g/molBenzaldehyde dimethyl acetal
CAS:Vegetable, nutty and floral flavour/fragrance
Fórmula:C9H12O2Pureza:Min. 95%Forma y color:Clear LiquidPeso molecular:152.19 g/mol3-Acetoxybenzoic acid
CAS:3-Acetoxybenzoic acid is a metabolite of 3-hydroxybenzoic acid, which is an intermediate in the biosynthesis of salicylic acid. It has been shown to have antibacterial properties and may be used as a topical treatment for skin infections caused by staphylococcus. 3-Acetoxybenzoic acid also has antiviral properties, which may be related to its ability to bind histone H3. 3-Acetoxybenzoic acid inhibits leishmania infantum growth and development by binding to chloride ions and preventing the formation of hydrogen bonds in the cell membrane. This prevents chloride ions from entering the cell and causes water channels to close, leading to dehydration and death.Fórmula:C9H8O4Pureza:Min. 95%Forma y color:PowderPeso molecular:180.16 g/mol3,5-Dibromo-4-methoxybenzonitrile
CAS:3,5-Dibromo-4-methoxybenzonitrile (DBMB) is a pentane that can be synthesized in the laboratory. DBMB is used as a weed control agent to kill weeds and grasses in neoprene rubber products and other materials. The chemical reacts with nitro groups on the surface of the material, producing an unstable intermediate that decomposes into pentane and nitric acid. 3,5-Dibromo-4-methoxybenzonitrile has been shown to have low toxicity to mammals at high doses. The compound may also be used as a chemical intermediate for the synthesis of other compounds or drugs. Nitro groups may be reduced by reductants such as sodium borohydride or lithium aluminium hydride to produce analdehyde derivatives.Fórmula:C8H5Br2NOPureza:Min. 95%Forma y color:White Off-White PowderPeso molecular:290.94 g/mol2,3,4-Trimethoxy-6-methylbenzaldehyde
CAS:2,3,4-Trimethoxy-6-methylbenzaldehyde is a synthetic coumarin with antibacterial activity. It is synthesized by the condensation of 3-hydroxyacetophenone and benzaldehyde. 2,3,4-Trimethoxy-6-methylbenzaldehyde has been shown to have antibacterial activity against both Gram-positive and Gram-negative bacteria. This molecule has also been shown to inhibit the growth of Gram negative bacteria in the presence of hydrogen peroxide. The crystal structure of this molecule was determined by XRD analysis and shows that it contains a dihedral angle of about 155°.Fórmula:C11H14O4Pureza:Min. 95%Peso molecular:210.23 g/mol2,6-Dichlorobenzaldehyde
CAS:2,6-Dichlorobenzaldehyde is a nucleophilic compound that has the ability to form hydrogen bonds. It reacts with phosphorus pentachloride to produce 2-chloro-4,6-dichlorobenzene. 2,6-Dichlorobenzaldehyde can be used in the synthesis of β-unsaturated ketones and anticancer drugs such as aziridines. It is also used as a precursor for coordination complexes. This compound is an efficient method for making nitrogen nucleophiles, which are important in chain reactions and the production of polymers. The 2,6-dichlorobenzaldehyde molecule contains two chiral centers that give rise to four stereoisomers. X-ray diffraction data shows that this molecule exists as a mixture of these four isomers.Fórmula:C7H4Cl2OPureza:Min. 97.5%Forma y color:PowderPeso molecular:175.01 g/mol2,4-Dimethoxybenzaldehyde
CAS:2,4-Dimethoxybenzaldehyde is a synthetic compound that has been shown to have activity against pancreatic lipase. It has been suggested as a potential drug for the treatment of metabolic disorders such as obesity or diabetes. 2,4-Dimethoxybenzaldehyde can be synthesized by reacting ethyl diazoacetate with an aldehyde in the presence of ammonium acetate. This chemical can also be used to produce ethyl esters and compounds belonging to the group of phlorotannins. 2,4-Dimethoxybenzaldehyde has been shown to have antioxidative activity and inhibitory effects on pancreatic lipase.
Fórmula:C9H10O3Pureza:Min. 95%Forma y color:White PowderPeso molecular:166.18 g/mol4-Amino-3-nitrobenzylamine hydrochloride
CAS:4-Amino-3-nitrobenzylamine hydrochloride is a potential vanilloid receptor antagonist with potent antagonistic activities. It has been shown to inhibit the activation of neuronal TRPV1 receptors, as well as the uptake of 4-aminobenzoic acid (4-BA) in rat brain synaptosomes. In addition, this compound can be used to optimize drug structure, acting as an amide and alkyl groups. 4-Amino-3-nitrobenzylamine hydrochloride binds to the vanilloid receptor TRPV1 and blocks its activation. This prevents the release of proinflammatory substances that are responsible for pain, inflammation, and tissue injury.Fórmula:C7H9N3O2·HClPureza:Min. 95%Forma y color:PowderPeso molecular:203.63 g/molMethyl 3-amino-4-chlorobenzoate
CAS:Methyl 3-amino-4-chlorobenzoate is an analog of 3-amino-4-chlorobenzoic acid. It is a multidrug that can cross the blood brain barrier and has been shown to have cytotoxic activity in vitro. Methyl 3-amino-4-chlorobenzoate has been postulated as a possible organometallic compound and may be synthesized through a chemical diversity approach. The chloride ion, which is present in methyl 3-amino-4-chlorobenzoate, has been shown to decrease the toxicity of nitrobenzoic acid, making this compound resistant to nitrosation reactions.Fórmula:C8H8ClNO2Pureza:Min. 95%Forma y color:PowderPeso molecular:185.61 g/mol(3-Hydroxy-4-methoxyphenyl)acetone
CAS:(3-Hydroxy-4-methoxyphenyl)acetone is a versatile building block that can be used as a reagent or in the synthesis of complex compounds. It is a useful intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. This compound also has the potential to serve as a scaffold for drug discovery.Fórmula:C10H12O3Pureza:(%) Min. 85%Forma y color:PowderPeso molecular:180.2 g/molGentisic acid sodium salt hydrate
CAS:Gentisic acid sodium salt hydrate is a benzoate that is used as a diagnostic agent in the study of inflammatory bowel disease. Gentisic acid sodium salt hydrate is a sodium salt of gentisic acid and has been shown to have anti-inflammatory properties. It is used as a stabilizer for solid dispersions, such as capsules, tablets, and granules. Gentisic acid sodium salt hydrate also has the ability to prevent degradation of certain drugs by hydrolysis or oxidation. Gentisic acid sodium salt hydrate can be synthesized from 2,6-dihydroxybenzoic acid (2,6-DHB) and hippuric acid.Fórmula:C7H5NaO4·xH2OPureza:Min. 98 Area-%Forma y color:White PowderPeso molecular:176.1 g/mol2-Ethoxy-4-nitrobenzoic acid
CAS:2-Ethoxy-4-nitrobenzoic acid is a nitrobenzoyl compound that is used as an anticoccidial drug. It has shown to be effective against coccidiosis in poultry. 2-Ethoxy-4-nitrobenzoic acid binds to the aminobenzoate moiety of the enzyme glutamic acid decarboxylase, thereby inhibiting its activity. This inhibits the production of lactic acid and leads to cell death by lack of energy. Amprolium is a coccidiostat that inhibits the synthesis of beta-alanine in cells, which leads to inhibition of protein synthesis and cell death.
Fórmula:C9H9NO5Pureza:Min. 95%Forma y color:PowderPeso molecular:211.17 g/mol3-Amino-2,4,6-triiodobenzoic acid
CAS:3-Amino-2,4,6-triiodobenzoic acid (3AIBA) is a chemical compound that is used as a contrast agent for medical imaging. It has been shown to be useful in the diagnosis of bladder cancer, and is used in the embolization of renal artery and ureteral calculi. 3AIBA functions by binding to the antigen binding sites on the tumor cells and allows visualization with X-rays. It has also been shown to be effective in reducing blood flow in tumors by blocking blood vessels with its cationic monomer. 3AIBA binds to the phosphate groups on DNA and causes crosslinking, which prevents DNA polymerase from binding with DNA. This inhibits DNA synthesis and cell division.Fórmula:C7H4I3NO2Pureza:Min. 95%Forma y color:PowderPeso molecular:514.83 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
Fórmula:C7H6O3Pureza:Min. 95%Forma y color:PowderPeso molecular:138.12 g/mol3-Hydroxybenzaldehyde
CAS:3-Hydroxybenzaldehyde (3HBA) is an organic molecule that belongs to the group of substituted benzaldehydes. It has been shown to induce muscle cell proliferation in vitro and in vivo, as well as increased levels of activated caspase-3 in vitro. 3HBA also has a high resistance to hydrochloric acid, hydrogen bond, and chemical structures. It also shows properties of intramolecular hydrogen bonding and aldehyde groups. 3HBA has been shown to be active against malonic acid-induced pulmonary edema in rats, which may be due to its ability to inhibit the release of erythrocytes from the bone marrow into the circulation.Fórmula:C7H6O2Pureza:Min. 96 Area-%Forma y color:Off-White PowderPeso molecular:122.12 g/molEthyl 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.Fórmula:C9H9ClO2Pureza:Min. 95%Forma y color:Clear LiquidPeso molecular:184.62 g/mol3-Acetylbenzonitrile
CAS:3-Acetylbenzonitrile is an isomeric, asymmetric synthesis that has been synthesised in the presence of copper complex and salicylic acid. The reaction was carried out with a gaseous phase, where the chalcone was formed. The experimental techniques used were cross-coupling reactions and molecular modeling techniques. 3-Acetylbenzonitrile has been synthesised by a rationalized enthalpic approach that includes alcohol dehydrogenases and molecular modeling techniques.Fórmula:C9H7NOPureza:Min. 95%Forma y color:PowderPeso molecular:145.16 g/mol4-Amino-3,5-dichlorobenzylamine dihydrochloride
CAS:4-Amino-3,5-dichlorobenzylamine dihydrochloride is a chemical intermediate that can be used as a reagent for the synthesis of other compounds. 4-Amino-3,5-dichlorobenzylamine dihydrochloride is considered to be a high quality chemical with versatile uses. It is listed in the Chemical Abstracts Service (CAS) registry under 164648-75-3, and can be obtained from various suppliers.Fórmula:C7H8Cl2N2·2HClPureza:Min. 95%Forma y color:PowderPeso molecular:263.98 g/mol2,4-Dimethylbenzoic acid
CAS:2,4-Dimethylbenzoic acid is a white solid with the chemical formula CH3C6H2O2. It is an organic acid that can be used as a building block in organic synthesis. The functional groups of 2,4-dimethylbenzoic acid are methyl and carboxyl. The most efficient method for the synthesis of 2,4-dimethylbenzoic acid is by reacting hydrochloric acid with dimethylaniline. This reaction can be carried out in one pot without isolation of intermediates. The structural analysis of 2,4-dimethylbenzoic acid was done using fluorescence lifetimes and hydrochloric acid. The reaction mechanism for the formation of 2,4-dimethylbenzoic acid from dimethylaniline is through a nucleophilic substitution reaction with chloride ion. Sample preparation for 2,4-dimethylbenzoic acid includes dissolution in water and filtration through a 0.45Fórmula:C9H10O2Pureza:Min. 95%Forma y color:White PowderPeso molecular:150.17 g/mol2-Amino-5-methylbenzoic acid
CAS:2-Amino-5-methylbenzoic acid is an anthranilic acid derivative that has been shown to have potent antitumor activity. It inhibits the growth of cancer cells and is effective against light emission. 2-Amino-5-methylbenzoic acid blocks the production of porphyrins, which are necessary for the production of heme, a cofactor in many enzymes. The compound also inhibits serine protease, which is involved in tumor cell proliferation and metastasis. 2-Amino-5-methylbenzoic acid has been shown to inhibit the growth of human liver cancer cells in vitro. This compound can be synthesized by a Suzuki coupling reaction with phenylacetic acid and 3-(2'-aminoethyl)aminobenzene.Fórmula:C8H9NO2Pureza:Min. 95%Forma y color:PowderPeso molecular:151.16 g/mol3,4-Diaminobenzoic acid
CAS:3,4-Diaminobenzoic acid is a compound that is produced by the condensation of two molecules of hydrochloric acid. 3,4-Diaminobenzoic acid has been used as a reagent in the synthesis of coumarin derivatives. This chemical has been shown to be an effective proton scavenger in an optimum concentration. Benzimidazole compounds are also synthesized from 3,4-diaminobenzoic acid and have been shown to be effective against autoimmune diseases. 3,4-Diaminobenzoic acid can be used for the production of diazonium salts, which are used in the synthesis of anti-inflammatory drugs and other pharmaceuticals. The hydroxyl group on this molecule makes it chemically stable and kinetic data shows that it has high diphenolase activity.Fórmula:C7H8N2O2Pureza:Min. 96 Area-%Forma y color:PowderPeso molecular:152.15 g/mol2,5-Dihydroxybenzaldehyde
CAS:2,5-Dihydroxybenzaldehyde is a compound that can be used as an antioxidant. It is also a precursor for the synthesis of benzalkonium chloride. 2,5-Dihydroxybenzaldehyde reacts with p-hydroxybenzoic acid to form 2,5-dihydroxyphenylacetic acid and benzoic acid. The reaction mechanism of 2,5-dihydroxybenzaldehyde has been studied in detail using hl-60 cells and has been shown to be significant cytotoxicity. The hydroxyl group in this molecule creates a hydrogen bond with the carbonyl group in p-hydroxybenzoic acid and the two react together to form products. This reaction is catalyzed by Michaelis–Menten kinetics and proceeds via an electrochemical detector. Nitrogen atoms are not present in this molecule but do exist in benzalkonium chloride, which is synthesized from 2
Fórmula:C7H6O3Pureza:Min. 95%Forma y color:Yellow PowderPeso molecular:138.12 g/mol2-Fluoro-3-methylbenzoic acid
CAS:2-Fluoro-3-methylbenzoic acid is a high quality, versatile building block that has been shown to be an effective reagent for the synthesis of complex compounds. It is also a useful intermediate in the synthesis of fine chemicals and speciality chemicals. This compound can be used as a reaction component for many chemical reactions, such as the formation of new bonds and the removal of protecting groups. As a versatile building block, 2-fluoro-3-methylbenzoic acid is an important starting material for synthesizing a number of natural products, pharmaceuticals, and other organic compounds.Fórmula:C8H7FO2Pureza:Min. 95%Forma y color:White PowderPeso molecular:154.14 g/mol2,5-Diaminobenzonitrile
CAS:2,5-Diaminobenzonitrile is a chemical compound with the molecular formula C6H5N3. It is a white crystalline solid that is insoluble in water and soluble in organic solvents such as acetone, chloroform, and ether. 2,5-Diaminobenzonitrile has been shown to be an effective monomer for polymer synthesis due to its stability and high densities. This chemical also has the ability to undergo hydrogen bonding and form hydrogen peroxide when heated to a temperature of 100 °C. The thermal isomerization of 2,5-diaminobenzonitrile can be slowed by adding other amines or nitrites.Fórmula:C7H7N3Pureza:Min. 95%Forma y color:PowderPeso molecular:133.15 g/mol5-Bromo-2-nitrobenzoic acid
CAS:5-Bromo-2-nitrobenzoic acid is a chemical compound that belongs to the group of bromonitrobenzenes. It is an important intermediate in organic chemistry and has been used as a reagent for the synthesis of various heterocyclic compounds. 5-Bromo-2-nitrobenzoic acid can be used as a building block for pharmaceuticals, agrochemicals, dyes, and other chemicals. This versatile chemical has been widely used in research and development as a reaction component for synthesizing pharmaceuticals or speciality chemicals or as a building block to produce useful scaffolds.
Fórmula:C7H4BrNO4Pureza:Min. 95%Forma y color:Slightly Yellow PowderPeso molecular:246.02 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.Fórmula:C7H6O4Pureza:Min. 95%Forma y color:PowderPeso molecular:154.12 g/mol2-Methoxy-4-aminobenzoic acid
CAS:2-Methoxy-4-aminobenzoic acid is a solute that can be used in the manufacture of pharmaceuticals. It has a high affinity for receptors and is potentially useful in the treatment of hypertension. 2-Methoxy-4-aminobenzoic acid has been shown to exhibit antihypertensive activity in animals by reducing cardiac output, systemic vascular resistance, and total peripheral resistance. The mechanism of action may be due to its ability to inhibit calcium ion influx into myocardial cells and block voltage-gated potassium channels. This drug also has an acidic pH, which makes it soluble in water. 2-Methoxy-4-aminobenzoic acid is insoluble in organic solvents such as hydrochloric acid or ether, which means it cannot be extracted from aqueous solutions by these solvents.Fórmula:C8H9NO3Pureza:Min. 95%Forma y color:Off-White PowderPeso molecular:167.16 g/mol1,3-Diphenylacetone
CAS:1,3-Diphenylacetone is a fine chemical that can be used as a building block for research chemicals, as a reagent in organic synthesis, or as a speciality chemical. It is also a versatile building block and has been shown to be useful in the formation of complex compounds. 1,3-Diphenylacetone can react with electrophiles to form new carbon-carbon bonds and has been used in reactions involving nucleophilic substitution, electrophilic addition, and Michael reactions. 1,3-Diphenylacetone is also water soluble and has been shown to be compatible with both ionic and covalent solvents.Fórmula:C15H14OPureza:Min. 99.0 Area-%Peso molecular:210.28 g/mol3-Methyl-4-nitrobenzonitrile
CAS:3-Methyl-4-nitrobenzonitrile is a fluorescing aromatic amine that is synthesized by aliphatic amines. It has been shown to inhibit the growth of cells in culture, which may be due to its ability to bind with and inhibit the insulin-like growth factor receptor-1 (IGF-1R). 3-Methyl-4-nitrobenzonitrile has also been shown to bind with cytochrome P450 enzymes, where it can be oxidized or reduced. The conformation of 3-methyl-4 nitrobenzonitrile is dependent on the solvent molecules present.Fórmula:C8H6N2O2Pureza:Min. 95%Forma y color:PowderPeso molecular:162.15 g/mol2-Amino-4,6-dimethoxybenzoic acid
CAS:2-Amino-4,6-dimethoxybenzoic acid is an organic chemical compound that can be used as a building block for the synthesis of other compounds. 2-Amino-4,6-dimethoxybenzoic acid has a number of uses including being a reagent in organic and inorganic reactions, such as the synthesis of dyes, pharmaceuticals, and pesticides. It is also used as a building block for complex compounds that are difficult to make. This chemical has been classified by the Chemical Abstract Services (CAS) registry with CAS number 21577-57-1.
Fórmula:C9H11NO4Pureza:Min. 95%Forma y color:Yellow SolidPeso molecular:197.19 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.
Fórmula:C7H5IO2Pureza:Min. 95%Forma y color:PowderPeso molecular:248.02 g/mol3,5-Diisopropyl-4-hydroxybenzoic acid
CAS:3,5-Diisopropyl-4-hydroxybenzoic acid is a white, crystalline compound that can be found as a dimer. It is soluble in solvents such as chloroform and ethers but insoluble in water. 3,5-Diisopropyl-4-hydroxybenzoic acid is used in the production of polyesters, polymers, and resins. This compound has been used to produce propofol and decarboxylating monomers for organic solvents. 3,5-Diisopropyl-4-hydroxybenzoic acid reacts with chloride ion at high temperatures to form chlorine gas and hydrogen chloride. The melting point of this compound is 169 degrees Celsius.Fórmula:C13H18O3Pureza:Min. 95%Forma y color:PowderPeso molecular:222.28 g/mol3-Bromo-5-hydroxybenzoic acid
CAS:3-Bromo-5-hydroxybenzoic acid is a metabolite of 3,5-dihydroxybenzoic acid (DHB) in the metabolism of benzoic acid. It has been shown to be an antibacterial agent and has been used to treat metabolic disorders in hamsters. Symptoms of 3-bromo-5-hydroxybenzoic acid include dyslipidemia, which can lead to metabolic disorders such as diabetes mellitus and atherosclerosis. The compound may also have a role in tuberculosis and cancer due to its ability to induce apoptosis.
Fórmula:C7H5O3BrPureza:Min. 95%Forma y color:White PowderPeso molecular:217.02 g/mol3-Nitrobenzoic acid methyl ester
CAS:3-Nitrobenzoic acid methyl ester is an organic compound that contains a hydroxyl group and a nitro group. It can be synthesized by the reaction of 3-nitrophenol and methanol in a solvent such as water or ethanol. The nitro group is important for the solvating power of this molecule, which has been shown to have approximations with other molecules. 3-Nitrobenzoic acid methyl ester is found in two different forms: the cis form and the trans form, which differ in the orientation of their nitro groups. The cis form is more stable than the trans form because it has a dipole moment. The vibrational frequencies are also higher for the cis form than for its trans counterpart. 3-Nitrobenzoic acid methyl ester has been shown to react with nintedanib, which is used to treat cancer, and inhibit kinetics. The kinetic data obtained from this study canFórmula:C8H7NO4Pureza:(Gc) Min. 98%Forma y color:PowderPeso molecular:181.15 g/mol2-Fluoro-4-nitrobenzoic acid methyl ester
CAS:2-Fluoro-4-nitrobenzoic acid methyl ester is a synthetic compound that has been shown to inhibit the activity of protein kinases and may be used as a lead compound for the development of allosteric inhibitors. A high yield synthesis of this compound was achieved using an allyl chloroformate, which is a versatile reagent that can be used to synthesize 2-fluoro-4-nitrobenzoic acid methyl ester. The structural analysis of this compound showed that it binds to the allosteric site on ATP binding proteins. This site is distinct from the active site and regulates ATP binding, hydrolysis, and phosphate transfer.Fórmula:C8H6FNO4Pureza:Min. 98%Forma y color:White PowderPeso molecular:199.14 g/mol2-Amino-4-methoxybenzoic acid
CAS:2-Amino-4-methoxybenzoic acid is a monophenolic compound that has been shown to have antioxidant properties. It is a redox potential with a pK of 7.8 and can be protonated at the phenolic hydroxyl group. 2-Amino-4-methoxybenzoic acid has been shown to inhibit the enzyme activities of histone proteins, which are enzymes that catalyze the formation of DNA from RNA. This compound also inhibits enzymes involved in amino acid synthesis such as anthranilate synthase and malic enzyme, as well as other enzymes such as phosphotransferase (PTS) and pyruvate kinase. 2-Amino-4-methoxybenzoic acid also causes inhibition of growth in phytophthora megasperma, an oomycete plant pathogen, by altering the redox potentials inside the cell membrane. The mechanism forFórmula:C8H9NO3Pureza:Min. 95%Forma y color:PowderPeso molecular:167.16 g/mol2,4-Dimethoxybenzoic acid
CAS:2,4-Dimethoxybenzoic acid is a phenolic compound that has been shown to bind to the ferrocene carboxylate of protocatechuic acid. The resulting complex was shown to be able to react with chloride ions in an acylation reaction. The kinetic study showed that the rate of reaction increased with increasing concentration of 2,4-dimethoxybenzoic acid. The protonation of 2,4-dimethoxybenzoic acid also increases its ability to react with chloride ions. This acidic compound can also react with amines and other compounds containing nitrogen in a similar manner as acetic anhydride. Addition of alkali hydrolysis may cause the cleavage of the hydrogen bond between 2,4-dimethoxybenzoic acid and protocatechuic acid, releasing 2,4-dimethoxybenzoic acid and protocatechuic acid.Fórmula:C9H10O4Pureza:Min. 95%Forma y color:White PowderPeso molecular:182.17 g/mol2,4-Dinitrobenzaldehyde
CAS:2,4-Dinitrobenzaldehyde is a chemical compound that contains a hydroxyl group and an amine. It is reactive and can form cationic surfactants with other compounds. 2,4-Dinitrobenzaldehyde has been shown to react with dimethyl fumarate in the presence of ethyl esters to form ethyl 2,4-dinitrophenolate. This reaction is catalyzed by dinucleotide phosphate and requires salinity or a base such as sodium methoxide. 2,4-Dinitrobenzaldehyde reacts with 2-aminoethanol in the presence of water or alcohols to produce 2,4-diaminobenzoic acid. The reaction mechanism for this process is not known but it may involve hydrogen bonding between the hydroxyl group and amine groups. 2,4-Dinitrobenzaldehyde has been used as a reagent for staining DNA in gel electFórmula:C7H4N2O5Pureza:Min. 95%Forma y color:PowderPeso molecular:196.12 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.Fórmula:C11H9NO4Pureza:Min. 95%Forma y color:White PowderPeso molecular:219.19 g/mol2,6-Dimethoxybenzoic acid
CAS:2,6-Dimethoxybenzoic acid is a chemical compound with the molecular formula of C9H8O4. It belongs to the group of sesquiterpene lactones and has been shown to have anti-inflammatory properties. 2,6-Dimethoxybenzoic acid exhibits a carboxylate reaction mechanism that can be activated by an enzyme, curculigoside, which hydrolyzes the ester bond in 2,6-dimethoxybenzoic acid. The reaction mechanism involves the group p2 (COOH) on 2,6-dimethoxybenzoic acid reacting with an alcohol on curculigoside to form an ester and protocatechuic acid. The dianthus caryophyllus plant produces 2,6-dimethoxybenzoic acid as a byproduct of its synthesis of protocatechuic acid. This compound is chemically studied using solid phase microextractionFórmula:C9H10O4Pureza:Min. 95%Forma y color:PowderPeso molecular:182.17 g/molOctyl gallate
CAS:Octyl gallate is a naturally occurring compound that belongs to the class of gallates. It is a non-toxic, water-soluble antioxidant that has been used as a preservative in foods and pharmaceuticals. Octyl gallate has been shown to inhibit nuclear DNA synthesis by binding to the dinucleotide phosphate (NDP) site on ribonucleotide reductase, thereby preventing the formation of deoxyribonucleotide triphosphates. A rate constant for this reaction has been determined using analytical methods. This compound also inhibits the growth of wild-type strains of Escherichia coli and Staphylococcus aureus, as well as some strains resistant to antibiotics such as erythromycin, chloramphenicol, tetracycline, and clindamycin. Octyl gallate may also have an effect on energy metabolism in bacteria by inhibiting p-hydroxybenzoic acid (PHBA) dehydratase
Fórmula:C15H22O5Pureza:Min. 95%Forma y color:White PowderPeso molecular:282.33 g/mol4-Ethylbenzonitrile
CAS:4-Ethylbenzonitrile is a chemical that is found in human lung. It is a terminal alkene, which undergoes aerobic photooxidation to form reactive oxygen species such as superoxide radical anion and hydrogen peroxide. 4-Ethylbenzonitrile is also converted to triazine, which has been shown to have tumorigenic properties in the lungs of rats and mice. The functional groups on 4-ethylbenzonitrile are amines, hydroxyls, carbonyls, and nitriles. This compound has an inhibitory effect on lung fibroblasts due to its ability to interfere with the function of β-unsaturated ketones. 4-Ethylbenzonitrile's basic structure contains three carbon atoms, two double bonds, and one triple bond.Fórmula:C9H9NPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:131.17 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.
Fórmula:C8H4ClF3O2Pureza:Min. 95%Forma y color:PowderPeso molecular:224.56 g/mol4-Bromo-3-methylbenzaldehyde
CAS:4-Bromo-3-methylbenzaldehyde is a versatile building block that is used in the synthesis of many complex compounds. It can be used as a reactant, reagent, or speciality chemical. 4-Bromo-3-methylbenzaldehyde is an intermediate for the production of other chemicals and has been shown to be useful in the synthesis of various scaffolds. This product has been shown to have high purity and quality.Fórmula:C8H7BrOPureza:Min. 95%Forma y color:Yellow PowderPeso molecular:199.04 g/mol3-Methyl-2-nitrobenzoic acid
CAS:3-Methyl-2-nitrobenzoic acid is a chemical that can be used for wastewater treatment. It has been shown to be effective against chlorantraniliprole, a pesticide that is often found in wastewater. 3-Methyl-2-nitrobenzoic acid also has the ability to reduce chloride levels by oxidizing it to produce chloride ions and nitrogen gas. This chemical can be used as an oxidation catalyst in wastewater treatment. 3-Methyl-2-nitrobenzoic acid has been shown to have photocatalytic activity with titanium dioxide and copper sulfate (CuSO4) under visible light illumination conditions.Fórmula:C8H7NO4Pureza:Min. 95%Forma y color:PowderPeso molecular:181.15 g/mol
