
Benzènes
Sous-catégories appartenant à la catégorie "Benzènes"
- Benzamides(62 produits)
- Acides benzoïques(5.474 produits)
- Alcools benzyliques(1.458 produits)
- Benzènes halogénés(33.965 produits)
- Phénols(2.654 produits)
11888 produits trouvés pour "Benzènes"
4-Chloro-3-hydroxybenzoic acid
CAS :4-Chloro-3-hydroxybenzoic acid (4-CHB) is a reactive compound that can be used for the detection of bacteria. 4-CHB reacts with peroxyl radicals in solution to form a chlorobenzoic acid derivative, which emits light when excited by radiation. 4-CHB is also capable of dehalogenating chlorobenzene, and can be used as a bioluminescent probe for the detection of bacteria. The reactions are efficient at low concentrations and are detectable with an ultraviolet or visible spectrophotometer.
Formule :C7H5ClO3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :172.57 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.Formule :C10H12O3Degré de pureté :(%) Min. 85%Couleur et forme :PowderMasse moléculaire :180.2 g/mol4-Hydroxybenzaldehyde
CAS :4-Hydroxybenzaldehyde is a phenolic compound that is produced in plants. 4-Hydoxybenzaldehyde is used as an extractant for sodium carbonate and hydroxyl group from acetate extract. The locomotor activity of animals was tested following administration of this substance, and it has been shown to have a high resistance against x-ray crystallography. The reaction mechanism for the formation of p-hydroxybenzoic acid from 4-hydroxybenzaldehyde has been proposed, which may be due to the oxidation of 4-hydroxybenzaldehyde by hydrogen peroxide. This reaction also induces apoptosis pathway in cells. Kinetic data for the reaction between 4-hydroxybenzaldehyde and hydrogen peroxide were obtained using UV spectroscopy.Formule :C7H6O2Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :122.12 g/molMethyl 2-bromobenzoate
CAS :Methyl 2-bromobenzoate is a chemical compound that can be used as a light emitting material. It is also used as a component of organic electrochemical cells (OECs) for the conversion of solar energy to electricity and can be used in the treatment of hepatitis. The reaction product is generated from the reaction of the halide with benzoate and light, which leads to an emission spectrum in the visible region. Methyl 2-bromobenzoate has been shown to be an efficient catalyst for Friedel-Crafts reactions, and it's pharmacokinetic properties have been studied in rats.
Methyl 2-bromobenzoate can also be used as a solid catalyst for the synthesis of bicyclic heterocycles.Formule :C8H7BrO2Degré de pureté :Min. 95%Couleur et forme :Colorless Clear LiquidMasse moléculaire :215.04 g/molo-Sulfobenzoic acid anhydride
CAS :o-Sulfobenzoic acid anhydride is a chemical that belongs to the class of inorganic acids. It is a white crystalline solid with a melting point of 107°C and can be found in its pure form or as sodium salts. o-Sulfobenzoic acid anhydride is stable when exposed to light and can be used in detergent compositions. It also has pharmacokinetic properties, which are affected by the presence of cationic polymers. This chemical is metabolized by microorganisms through hydrogen bonding interactions and has been shown to have antimicrobial activity against infectious bacteria, such as erythromycin-resistant strains of Staphylococcus aureus and Mycobacterium tuberculosis.
Formule :C7H4O4SDegré de pureté :Min 98%Couleur et forme :Slightly Brown PowderMasse moléculaire :184.17 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
Formule :C15H22O5Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :282.33 g/molMesitaldehyde - 97%
CAS :Mesitaldehyde is a diazonium salt that is synthesized by the reaction of nitrosyl chloride and sodium carbonate in an acidic solution. This chemical has been studied for its potential use as a therapeutic drug due to its ability to inhibit the enzyme dpp-iv, which is involved in the development of diabetic neuropathy. Mesitaldehyde has also been shown to be an inhibitor of malonic acid, ethylmalonic acid and other organic acids. The analytical method for mesitaldehyde involves hydrolyzing the product with hydrochloric acid in order to produce ethylmalonic acid, which can then be quantified using spectrophotometry.Formule :C10H12ODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :148.2 g/mol2-Hydroxy-6-methoxybenzaldehyde
CAS :2-Hydroxy-6-methoxybenzaldehyde is a molecule that can form hydrogen bonds with other molecules. FT-IR spectroscopy has shown that this compound has a copper complex and an acidic proton, which may be due to intramolecular hydrogen bonding interactions. The compound also has been shown to have potent inhibitory activity against cellular growth and cancer cells in vitro. 2-Hydroxy-6-methoxybenzaldehyde is a metal chelator and can therefore bind to metals such as iron and copper. It is genotoxic, which means it damages DNA by causing DNA strand breaks or crosslinks, leading to cell death. This chemical may also cause genetic mutations through the formation of tautomers that make DNA replication difficult. Gel chromatography shows that 2HMB has a low molecular weight (MW) and high solubility.Formule :C8H8O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :152.15 g/mol4-iso-Propoxybenzoic acid
CAS :4-iso-Propoxybenzoic acid is a synthetic compound with antimycobacterial activity. It is an active form of 4-iso-propoxybenzoic acid that has been shown to potently inhibit the growth of Mycobacterium tuberculosis and other mycobacteria. The formyl group in the structure of this compound enables it to bind to DNA, RNA, and proteins and disrupts their synthesis. This chemical also has the ability to cross cell membranes, which may contribute to its potent activity. This drug has been industrially produced by solid phase synthesis techniques.
Formule :C10H12O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :180.2 g/molEthyl 4-bromobenzoate
CAS :Ethyl 4-bromobenzoate is a halide that can be synthesized by the cross-coupling reaction with an aryl halide and a boronic acid. This synthesis has been used successfully to prepare benzoates, which are generally more difficult to synthesize than boronic acids. The coupling reaction of ethyl 4-bromobenzoate with an aryl halide and a boronic acid in the presence of copper as catalyst yields ethyl 4-bromobenzoate in high yield. A synergistic interaction occurs between the two reagents, leading to significant cytotoxicity in vitro. This property may be due to the light emission from this compound when it is exposed to ultraviolet light. Ethyl 4-bromobenzoate is also able to inhibit aerobic glycolysis and cancer cell growth in vitro through its ability to inhibit the activity of phosphofructokinase 1 (PFK1Formule :C9H9BrO2Degré de pureté :Min. 97.5 Area-%Couleur et forme :Clear LiquidMasse moléculaire :229.07 g/mol2,3,4-Trimethoxybenzoic acid
CAS :2,3,4-Trimethoxybenzoic acid is a molecule that has been shown to stimulate epidermal growth. It is a methylating agent that can be used to produce 2-hydroxybenzoic acid from protocatechuic acid. The hydroxy group on the 2,3,4-trimethoxybenzoic acid binds to the chloride ion in the protocatechuic acid and removes it from the molecule. This reaction mechanism is supported by x-ray crystal structures of protocatechuic acid and 2,3,4-trimethoxybenzoic acid.Formule :C10H12O5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :212.2 g/mol2-Hydroxy-4-methoxybenzaldehyde
CAS :2-Hydroxy-4-methoxybenzaldehyde is an antifungal agent that has been shown to have a broad spectrum of activity against filamentous fungi. It is able to inhibit the growth of fungi by inhibiting the enzyme shikimate dehydrogenase, which is involved in the synthesis of aromatic amino acids and other essential metabolites. 2-Hydroxy-4-methoxybenzaldehyde also inhibits xylose reductase and alpha-galactosidase, enzymes that are involved in cell wall biosynthesis. This compound is effective against Candida albicans, Aspergillus niger, and Trichophyton mentagrophytes. 2-Hydroxy-4-methoxybenzaldehyde has also been shown to have bacteriostatic effects on Escherichia coli.
Formule :C8H8O3Degré de pureté :Min. 95%Couleur et forme :Off-White PowderMasse moléculaire :152.15 g/mol3-Formyl-4-hydroxybenzoic acid
CAS :3-Formyl-4-hydroxybenzoic acid is a synthetic compound with anticancer activity. It is an azobenzene that has been shown to have photocatalytic activity. 3-Formyl-4-hydroxybenzoic acid has a carboxylate functional group and the ethyl ester functional group. The anticancer activity of this compound may be due to hydrogen bonding interactions, as well as its ability to cause DNA damage in cells by photolysis and its antiviral potency.Formule :C8H6O4Degré de pureté :90%Couleur et forme :White PowderMasse moléculaire :166.13 g/mol2,4,6-Trimethylbenzoic acid
CAS :2,4,6-Trimethylbenzoic acid is a molecule that belongs to the class of carboxylates. It has been shown to exhibit anticarcinogenic properties in patients with cervical cancer. 2,4,6-Trimethylbenzoic acid inhibits the growth of cervical cancer cells by blocking the activation of ferrocenecarboxylic acid (FCCA). This compound also blocks the activity of hydrogen bond and nitrogen atoms that are essential for cell division and development. 2,4,6-Trimethylbenzoic acid is used as an intermediate in the production of ferrocene derivatives. It can be used for acylation reactions with aromatic or aliphatic amines under acidic conditions.
Formule :C10H12O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :164.2 g/molEthyl homovanillate
CAS :Inhibitor of monoamine oxidase AFormule :C11H14O4Degré de pureté :Min. 95%Couleur et forme :Colorless PowderMasse moléculaire :210.23 g/mol3,4-Dihydroxybenzaldehyde
CAS :3,4-Dihydroxybenzaldehyde is an active compound that is a protocatechuic aldehyde. It has been shown to inhibit protein oxidation and kidney injury. 3,4-Dihydroxybenzaldehyde also inhibits the production of bcl-2 protein and growth factor-β in rat urine. This compound has been used in Chinese medicinal preparations as well as in control methods for oxidizing agents.
Formule :C7H6O3Couleur et forme :Brown White PowderMasse moléculaire :138.12 g/mol3,4-Dihydroxybenzylamine hydrobromide
CAS :3,4-Dihydroxybenzylamine hydrobromide is a chemical that reacts with hydrogen peroxide to produce light. It is used as a nutrient for the chemiluminescent reaction in a nutrient solution to detect dopamine, chlorogenic acids, and trifluoroacetic acid. 3,4-Dihydroxybenzylamine hydrobromide can also be used as an analytical method for the measurement of cortisol concentration in plasma and saliva samples. This chemical analogically reacts with monoamine neurotransmitters such as dopamine and gamma-aminobutyric acid (GABA) to form fluorescent probes. 3,4-Dihydroxybenzylamine hydrobromide is not toxic or mutagenic and has been shown to be safe for use in humans.Formule :C7H10BrNO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :220.06 g/mol3,4-Dihydroxy-6-nitrobenzaldehyde
CAS :3,4-Dihydroxy-6-nitrobenzaldehyde is a nitrite that can be used to produce nitric acid. It can also be used in the synthesis of caffeic acid and protocatechuic aldehyde. This molecule is also a catalyst for the conversion of 3,4-dihydroxybenzoic acid to chloride and purine derivatives. 3,4-Dihydroxy-6-nitrobenzaldehyde is nucleophilic and can react with an electron pair donor such as methyl ester or dimerization. The product of this reaction is an unsaturated compound called hyperuricemic mice.Formule :C7H5NO5Degré de pureté :Min. 95%Couleur et forme :Yellow PowderMasse moléculaire :183.12 g/mol3,5-Dichloro-4-hydroxybenzaldehyde
CAS :3,5-Dichloro-4-hydroxybenzaldehyde is a triiodomethane derivative that reacts with chlorine to form a chlorinated aldehyde. It is used as an intermediate in the production of 4-hydroxybenzoic acid from phenylacetic acid and 4,4'-dichlorodiphenyl sulfone. 3,5-Dichloro-4-hydroxybenzaldehyde can be decarboxylated at elevated temperatures to produce formic acid. This compound has been used in wastewater treatment as it can remove chlorine byproducts and other pollutants such as nitrates, nitrites, and iron ions. The reaction kinetics of 3,5-dichloro-4-hydroxybenzaldehyde have been studied using hydroxymethyl groups and formyl groups to determine the rate of demethylation. The rates were found to be dependent on temperature.Formule :C7H4Cl2O2Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :191.01 g/molEthyl 4-(N,N-diethylamino)benzoate
CAS :Ethyl 4-N,N-diethylamino)benzoate is a molecule that contains a carbonyl group. In an exothermic reaction, the carbonyl group reacts with naphthalene in the presence of activated alkyl substituents to form a fluorescent product. The molecule has a constant and is monomeric. It has an aromatic hydrocarbon structure, which results in a red shift in the fluorescence emission spectrum. Ethyl 4-N,N-diethylamino)benzoate reacts with solvents such as water and alcohols to form solutes that are fluorescent.Formule :C13H19NO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :221.3 g/mol
