Benzyl alcohols

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

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

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

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.

4-Iodo-2-nitrophenol is a halophenol that is used in the production of drugs such as anti-inflammatory agents, antiviral agents, and immunosuppressants. 4-Iodo-2-nitrophenol has been shown to bind to an antigen and stimulate the production of growth factors. 4-Iodo-2-nitrophenol also binds to hif1α, which is a transcription factor that regulates the expression of genes involved in cellular response to low oxygen conditions. Covid -19 pandemic influenza virus uses 4-iodo-2 nitrophenol as a substrate for its replication. This means that this drug can be used as an inhibitor for covid -19 pandemic influenza virus.

2,4-Dimethoxybenzyl alcohol is a functional group that is used in organic synthesis. It can be synthesized from the reduction of 2,4-dichlorobenzaldehyde with sodium borohydride or lithium aluminum hydride. The compound is used to synthesize hydroxamic acids and it has shown photocatalytic activity. 2,4-Dimethoxybenzyl alcohol is also used as an intermediate for the synthesis of octamers and trifluoroacetate esters. Other uses include its ability to induce chloride secretion by inhibiting the chloride ion channel in the cell membrane and its ability to inhibit quinoline derivatives such as indolocarbazoles. 2,4-Dimethoxybenzyl alcohol has been shown to have inhibitory activities against a number of biological targets including growth regulators and enzymes (i.e., stereoselective). 2,4-Dimethoxybenzyl alcohol has

4,4'-Oxydiphenol is an organic compound that contains a phenolic hydroxyl group. The molecule is activated by the presence of an electron withdrawing group such as a carbonyl or sulfonate. This activation allows for nucleophilic attack on the carbon-carbon double bond to form a new bond. 4,4'-Oxydiphenol can also be synthesized from ethane and epichlorohydrin in the presence of a base such as sodium methoxide. The resulting product is a polyester with resistive properties due to its high molecular weight and low solubility.

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.

2-Amino-4-methylphenol is an organic compound that belongs to the group of p2 molecules. It has been shown to react with hydroxyl radicals in the human liver, and this reaction may be a significant mechanism for its toxicity. 2-Amino-4-methylphenol also reacts with low concentrations of hydrochloric acid (0.1 M) to form a stable intermediate with an intramolecular hydrogen bond between the amine nitrogen and the carbonyl carbon. This intermediate then reacts with more hydrochloric acid to form 4-(hydroxymethyl)benzoic acid and 2-aminoethanol. The NMR spectra of 2-amino-4-methylphenol show only one resonance due to the absence of electronegative groups on the molecule, which makes it resistant to oxidation by air or light. The high resistance of 2-amino-4-methylphenol makes it an ideal chemical

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