Alcools benzyliques

Benzyl alcohol (Benzenemethanol), a colorless liquid, is an aromatic alcohol with a mild pleasant aromatic odor.

<p>Applications Cyclohexanemethanol is a chemicl reagent used in the synthesis of potent inhibitors of cyclin-dependent kinases 1 &amp; 2.<br>References Hardcastle, I. et al.: J. med. Chem., 47, 15, 3710 (2004); Sayle, K. et al.: Bioorg. Med. Chrm. Lett., 13, 3079 (2003);<br></p>

<p>Applications α-Toluenol is used in the synthesis of Cephalosporolide B as a versatile biomimetic synthetic precursor for chemical synthesis of other cephalosporides.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Song, L. et al.: Org. Lett., 15, 5850 (2013);<br></p>

<p>Applications This compound contains up to 25% of the two other regioisiomers.<br></p>

<p>Stability Hygroscopic<br>Applications Benzyl Alcohol (D7, 98%) (cas# 71258-23-6) is a useful research chemical.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br></p>

<p>3,3'-Dichlorobisphenol A is a chlorine-containing organic compound that is used in the manufacture of polycarbonate plastics. It has been found to be genotoxic and carcinogenic in animals. 3,3'-Dichlorobisphenol A is also toxic to aquatic organisms and may persist for long periods in the environment. 3,3'-Dichlorobisphenol A enters wastewater when it is released during the production of polycarbonate plastics or as a byproduct of other chlorination reactions. The most common method for removing 3,3'-dichlorobisphenol A from wastewater is to use UV irradiation followed by chlorine gas treatment. This process can lead to the formation of additional chlorinated compounds that are more toxic than 3,3'-dichlorobisphenol A.</p>

<p>3-Methoxyphenol is a chemical that is used in the treatment of wastewater. It has been shown to have antibacterial and antiviral properties, as well as the ability to prevent bowel disease. 3-Methoxyphenol can be used to treat metal hydroxides by reacting with them and converting them into metal oxides. The reaction mechanism of 3-methoxyphenol has been best studied using coumarin derivatives, which are structurally similar to 3-methoxyphenol.<br>The ester hydrochloride salt form of 3-methoxyphenol is a prodrug that is metabolized by cytochrome P450 enzymes in the liver via an esterase pathway. This prodrug may be especially useful for patients with bowel disease or low levels of cytochrome P450 enzymes, such as those with chronic kidney failure or AIDS.<br>3-Methoxyphenol has been shown to inhibit Jak</p>

<p>Chlorphenesin carbamate is a centrally acting muscle relaxant, which is a synthetic compound derived from chlorphenesin.</p>

<p>3-Ethoxyphenol is an organic compound that has a phenolic hydroxyl group attached to the 3-position of an ethyl alcohol. The ethoxy groups on the molecule allow it to bind to receptors in the central nervous system, including the dopamine receptor and the d4 receptor. This binding process is thermodynamically and kinetically favorable, which leads to a high metabolic rate. 3-Ethoxyphenol has been shown to have strong antiviral properties, particularly against chromobacterium violaceum, and can be used as a specific ligand for metal surfaces. The coumarin derivatives of 3-ethoxyphenol have also been shown to inhibit the growth of propionate and covid-19 pandemic.</p>

<p>2-Bromophenol is a sodium salt that can be prepared by the reaction of sodium hydroxide with 2-bromoaniline. It is an inhibitor of acetylcholinesterase, which has been shown to be effective in treating Alzheimer's disease and other neurodegenerative disorders. 2-Bromophenol has been shown to inhibit the polymerase chain reaction (PCR) in human serum and mitochondrial membrane potential, as well as electrochemical impedance spectroscopy. It also inhibits the formation of intramolecular hydrogen bonds during the catalytic cycle of acetylcholinesterase.</p>

<p>3-Chloro-2-nitrobenzoic acid is a chemical compound that is used in the synthesis of quinoline derivatives. It has been shown to be genotoxic and cytotoxic in cell culture. 3-Chloro-2-nitrobenzoic acid binds to DNA, forming a covalent bond with the nitrogen atoms in the DNA bases. This binding may lead to changes in the structure of DNA, which could potentially be mutagenic. 3-Chloro-2-nitrobenzoic acid also has an optical absorption maximum at around 260 nm, which is indicative of hydrogen bonding between molecules.<br>3-Chloro-2-nitrobenzoic acid has been shown to inhibit brain cells and lung cells by interfering with cellular respiration and mitochondrial function.</p>

<p>Standard for determination of toxic monomers from polymer coatings</p>

<p>4-Aminothiophenol is a redox potential probe that is used as an analytical chemistry reagent. It has been shown to react with nitrite ion and form a nitrogen atom, which can be detected by Raman spectroscopy. 4-Aminothiophenol has also been used to measure the amount of fatty acid in human serum samples. 4-Aminothiophenol has been shown to have an enhancement effect on the detection sensitivity of model system reactions and can be used as a model system for these reactions. The reaction mechanism for this compound is not well understood, but it is believed that it may involve electron transfer from the aminothiophenol radical cation to the nitrite ion.</p>

<p>4-Bromobenzyl alcohol is a reactive chemical that reacts with water to form the hydroxyl group and hydrogen bond. It has been shown to inhibit the reaction of ethyl formate with biphenyl by cleaving the molecule and forming a new site specific. Magnetic resonance spectroscopy has been used to study the reactivity of 4-bromobenzyl alcohol in model systems. The reaction mechanism is thought to be similar to that of 2-bromoethanol, which is an inhibitor molecule for this process. 4-Bromobenzyl alcohol's magnetic resonance spectrum shows proton peaks at 3.02 ppm, 2.19 ppm, and 1.77 ppm, as well as a signal at 8.03 ppm corresponding to the hydroxyl group.</p>

<p>3-Methoxybenzyl alcohol is a natural product from the root of the orchid Dendrobium officinale. It has been shown to inhibit the growth of bacteria by binding to the enzyme Aldehyde Dehydrogenase, which is required for cellular energy production. The product also inhibits bacterial Vanillyl Alcohol Dehydrogenase, which prevents the formation of vanillin. 3-Methoxybenzyl alcohol has a neutral pH and can be used as an antimicrobial agent in acidic foods and beverages. 3-Methoxybenzyl alcohol also has antioxidant properties, and has been shown to prevent damage from oxidative stress.</p>

<p>2,3-Dimethoxybenzyl alcohol is a fine chemical that is used as an intermediate in the synthesis of other chemicals. It has been shown to be a useful scaffold for the development of new compounds and is also a versatile building block for the synthesis of complex molecules. This compound exhibits many special properties that make it useful in research and industrial processes. It is a high quality reagent that can be used in organic syntheses and as a reaction component.<br> 2,3-Dimethoxybenzyl alcohol has been shown to have antiviral activity against HIV-1, HIV-2, SIV mac1, and VSV.</p>

<p>4-Bromo-2,6-di-tert-butylphenol is a chemical compound. It is a yellow solid with an optical rotation of +42.8° (c=0.5, methanol). The molecular weight is 270.4 g/mol and the density is 1.06 g/cm3. The chemical formula is C11H14Br2O4. This compound can be prepared from 2,6-di-tert-butylbenzaldehyde by reaction with bromine in the presence of alkali or from 4,4′-biphenol by reaction with bromine in the presence of sodium hydroxide in ethanol. The compound exists as two enantiomers: R-(+)-4-Bromo-2,6-di-tert-butylphenol and S-(-)4-Bromo-2,6,-di tert butylphenol. Optical activity</p>

<p>Mild antiseptic agent</p>

<p>2,4,6-Trimethylbenzyl alcohol is an efficient method for the production of 2,4-dimethoxybenzaldehyde and 2,6-dimethoxybenzaldehyde. It can be used with ferrite as a dehydrogenative catalyst to produce hydroxymethyl groups in the presence of acid catalysts. The oxidation products of 2,4,6-trimethylbenzyl alcohol are polymers that have been shown to stabilize aldehydes and primary alcohols. This compound also has been shown to desymmetrize aromatic hydrocarbons and is capable of catalysis.</p>

<p>2,6-Dimethoxyphenol is a chemical compound that is used in the manufacture of industrial chemicals. It is also used as an intermediate in organic synthesis and has been shown to have antibacterial activity against some strains of bacteria. 2,6-Dimethoxyphenol binds to bacterial ribosomes by interfering with the protein synthesis machinery. The reaction mechanism occurs via a nucleophilic attack by the hydroxyl group on the carbonyl carbon atom, leading to a tetrahedral intermediate with the coordination geometry of square planar. This compound has been shown to scavenge anion radicals and has high resistance to oxidation from redox potential.</p>

<p>4-Ethoxybenzyl alcohol is a reactive compound that can be photoexcited. It has been shown to have a cavity and is able to absorb light of wavelengths between 250 nm and 500 nm. 4-Ethoxybenzyl alcohol reacts with various compounds, such as aldehydes, to form new compounds. It has been shown that the reaction system can be used for high-throughput analysis, which may lead to the discovery of new drugs. It also has been found that 4-ethoxybenzyl alcohol can react with sulfates in an organic solvent to produce sulfonates. This reaction system has potential for use in the production of new drugs or other chemical products.</p>

<p>2,6-Dimethyl-4-cyanophenol is a pyrimidine compound that has been used as a pharmaceutical drug to inhibit the replication of human immunodeficiency virus (HIV). It has also been shown to be effective against the strains of HIV that are resistant to other drugs. 2,6-Dimethyl-4-cyanophenol is an inhibitor of reverse transcriptase, which is an enzyme necessary for the production of viral DNA from viral RNA. This drug also inhibits bacterial growth by binding to bacterial DNA gyrase and topoisomerase IV. 2,6-Dimethyl-4-cyanophenol has a number of functionalities: it can act as an acid or base depending on its environment and it can form hydrogen bonding interactions with other molecules. This drug also has acidic properties that make it useful in the treatment of ph problems caused by trifluoroacetic acid.</p>

<p>Blue redox dye; used to quantify vitamin C content</p>

<p>3-Hydroxybenzyl alcohol is a fatty acid with a hydroxyl group. The clinical relevance of 3-hydroxybenzyl alcohol remains unclear. It has been used in acetate extract and ph optimum tests, as well as to study reaction solutions and nmr spectroscopic data. Hydrogen bonds have been observed between the molecule's hydroxyl group and the oxygen atoms in water molecules, which may explain its antifungal properties. 3-hydroxybenzyl alcohol also has an inhibitory effect on cyclic peptide synthesis, rotarod test performance, and analytical methods. It is a broad-spectrum antimicrobial that can be used against bacteria, fungi, protozoa and viruses. 3-hydroxybenzyl alcohol has an acidic character because it reacts with copper ions to form a copper complex.</p>

<p>Blue dye in sample buffers for protein and DNA electrophoresis; pH indicator</p>

1,2,4-Benzenetriol (BNT) is a reactive molecule that has been shown to have hydrogen bonding interactions with copper chloride. It has been proposed as an inhibitor of methyltransferase, which is involved in the synthesis of methionine. Studies have shown that BNT can also inhibit iron homeostasis and transfer reactions. The x-ray diffraction data for this compound shows that it forms a complex with the hydroxyl group. This complex is stabilized by hydrogen bonding interactions with the hydroxylic proton of the 1,2,4-benzenetriol molecule. BNT has been shown to be toxic to HL-60 cells and K562 cells at concentrations greater than 5 mM. It has also been found to be effective against chlorogenic acids and other compounds in energy metabolism studies at concentrations between 0.5 and 2 mM.

<p>3-Ethoxy-4-hydroxybenzyl alcohol (EHBA) is a functional gene that has been shown to have anti-oxidant properties. EHBA is capable of scavenging free radicals and reactive oxygen species, and is therefore thought to be a potential treatment for diseases caused by peroxide and aldehydes. It has also been shown to reduce the production of vanillyl alcohol, which is associated with pain in tissues such as the trigeminal nerve. The anti-oxidant properties of EHBA are thought to be due to its ability to inhibit lipid peroxidation, protein oxidation, and DNA damage. EHBA can be administered orally or topically.</p>

Component of polymer coatings in food cans; toxic contaminant

<p>2,4-Dimethylbenzyl alcohol is a primary alcohol that is found in many natural products. It is a functional group that can be used as a chemical intermediate or an intermediate for the production of other compounds. 2,4-Dimethylbenzyl alcohol has been shown to have genotoxic activity and can cause DNA damage. This compound has been found in adipose tissue and functions by inhibiting the uptake of pyrethroid insecticides by adipose cells. This compound has also been shown to be oxidized into several different oxidation products that are all isomeric with each other, including 2,6-, 3,5-, and 4,6-dimethylbenzaldehyde. These oxidation products may be esterified with conjugates such as glucuronic acid or sulfate which may aid in its absorption through the gut wall into the bloodstream.</p>

<p>3-Formylbenzyl alcohol is a fatty acid that has been shown to inhibit the growth of bacteria by binding to the hydroxyl group of the bacterial cell membrane. 3-Formylbenzyl alcohol's antimicrobial activity is due to its ability to inhibit the production of fatty acids in the cell membrane, preventing the formation of an outer layer that protects bacteria from attack. The antibacterial agent also inhibits protein synthesis and prevents DNA replication, resulting in cell death. 3-Formylbenzyl alcohol binds to bacteria through hydrogen bonding and has been shown to be effective against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. The mechanism for this action is not clear but may involve an intramolecular hydrogen bond or nucleophilic attack by one of its carbonyl groups on a nitrogen atom in the bacterial molecule.</p>

<p>3,4,5-Trimethoxyphenol is a fruit extract that has been shown to inhibit the activity of protein synthesis. It also inhibits the replication of hepatitis C virus in vitro by interfering with the acylation reaction and preventing the attachment of lipoproteins to cell membranes. 3,4,5-Trimethoxyphenol may be used as an analytical reagent for determining the degree of unsaturation in cinnamic acid derivatives.</p>

<p>4-Iodo-2-methylphenol is an antiobesity drug that is a synthetic derivative of 4-iodoaniline. It has been shown to bind to the receptor y181c, which is found on the surface of fat cells. The ligand, which is a specific chemical structure that binds to this receptor, may be able to block the uptake of lipids by fat cells, thereby reducing body weight and cholesterol levels. 4-Iodo-2-methylphenol also has sulfide groups that make it more soluble in water than other similar drugs. This makes it more easily absorbed into the bloodstream and may allow for lower doses. 4-Iodo-2-methylphenol also has an affinity for naphthalene, which may be useful in removing toxic chemicals from the environment.</p>

<p>4-Cyano-3-fluorophenol is a chemical compound that has two phenoxy groups and one fluorine atom. 4-Cyano-3-fluorophenol has been shown to be an effective antagonist of GABA A receptors, which may be due to its ability to interact with the chloride ion site on the receptor, or its hydrogen bonding effects with the receptor. 4-Cyano-3-fluorophenol has been shown to have potent effects in a number of other biological systems. These include inhibition of suzuki coupling reactions (a type of nucleophilic substitution reaction), as well as acylation reactions in which an acid reacts with an alcohol to form an ester, and pharmacokinetic properties. 4-Cyano-3-fluorophenol also has been shown to bind selectively to proteins, including those involved in protein–protein interactions.</p>

<p>2-Amino-5-fluorophenol (2AP) is a natural product that has been found to be an effective inhibitor of the enzyme fatty acid synthase. 2AP has been shown to inhibit the growth of Candida albicans, Trichophyton mentagrophytes, and Toxoplasma gondii in a model system. This compound is used as a starting material for the synthesis of other pharmaceutical compounds, such as fluoroquinolones and aminoglycosides. 2AP inhibits the activity of the enzyme fatty acid synthase by binding to the thiolate moiety on cysteine residues near the active site and thus preventing substrate binding. This inhibition results in a decrease in fatty acid synthesis, which leads to cell death.</p>

<p>4-Chlorobenzyl alcohol is a lipase inhibitor that is used in the treatment of pancreatic disorders. It binds to the active site of pancreatic lipase, which prevents the enzyme from hydrolyzing the ester bonds of glycol esters and long chain fatty acids, thereby inhibiting their absorption. This product does not inhibit other enzymes (e.g., amylase) or have an effect on chloride secretion. The reaction with 4-chlorobenzyl alcohol can also be catalyzed by hydrogen bonding between the carboxylic acid group and a hydroxyl group. Miconazole nitrate is a synthetic antifungal agent that inhibits ergosterol synthesis by binding to 14-alpha demethylase, which converts lanosterol into ergosterol. It has been shown to inhibit the growth of fungi such as Candida albicans and Aspergillus niger when combined with 4-chlorobenzyl alcohol. Cleavage products</p>

<p>3,5-Dihydroxybenzyl alcohol is an organic solution that has been shown to inhibit the growth of cancer cells by binding to the chloride ion and forming a hydrophobic effect with the hydrochloric acid. This compound also inhibits the growth of other cells such as bacteria and yeast. 3,5-Dihydroxybenzyl alcohol has potent inhibitory activity against silver ions and prevents their adhesion to DNA molecules. The molecule also has a hydroxyl group which may help to prevent bacterial growth by preventing the production of proteins essential for cell division. 3,5-Dihydroxybenzyl alcohol is not toxic to human liver cells and does not cause any carcinogenic effects in vitro.</p>

<p>3,4-Dinitrobenzyl alcohol is a synthetic chemical that is used as an intermediate for the synthesis of other chemicals. It is a dipole with a molecular weight of 188.2 g/mol and has two substituents. 3,4-Dinitrobenzyl alcohol is produced by the oxidation of 3,4-dichlorobenzyl alcohol with nitric acid and sulfuric acid. This process occurs in industrial settings to produce dyes, perfumes, and medicines. 3,4-Dinitrobenzyl alcohol is used as a starting material for the production of other compounds that are used in the textile industry or as insecticides.</p>