Alcools benzyliques

2,5-Dimethylbenzyl alcohol is a colorless to pale yellow liquid used primarily in the manufacture of perfumes. It is also used as a solvent and an intermediate in organic synthesis. This chemical has been shown to be taken up by adipose tissue and excreted in urine as glucuronide conjugates. 2,5-Dimethylbenzyl alcohol is metabolized into 5-methylbenzaldehyde and then further into 2-methoxy-5-methylbenzaldehyde (2MMB). The final metabolic product of 2,5-dimethylbenzyl alcohol is benzoic acid.

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

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.

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.

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.

2-Chloro-4-nitrophenol (2CP) is a chemical that has been found to be an optical sensor for nitrite ion. It reacts with nitrite ion at a pH of 5 and changes its color from yellow or orange to red. 2CP is also an antimicrobial agent and has shown biological properties against bacteria, including the ability to inhibit bacterial growth and reduce the number of bacteria in human serum. The optimum concentration for the inhibition of bacterial growth was found to be 0.5 mg/mL, which is much lower than the concentration used in other studies. The genus, bacterial strain, and pH were all found to influence the activity of 2CP against bacteria. Process optimization trials have shown that 4-hydroxycinnamic acid can be used as an alternative substrate for 2CP's reaction with nitrite ion. Monoclonal antibodies were also developed that are specific for transfer reactions with nitrate ion and can be used as a detection system for nit

2-Amino-4-nitrophenol is a chemical compound that has been used in the modeling of hydrogen bonds. It is also used as a reagent for the determination of the concentration of hydrochloric acid and sodium carbonate. 2-Amino-4-nitrophenol is activated with hydrochloric acid and then reacts with sodium carbonate to produce a yellow solution. The solution's colour changes with pH, which can be determined by measuring the absorption at different wavelengths on an nmr spectrometer. Nitro groups are present in 2-amino-4-nitrophenol, which may cause allergic reactions. This chemical also has an acidic nature due to its inorganic acid properties.

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.