Benzyl alcohols

<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 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>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.</p>

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

<p>2-Fluoro-4-nitrophenol is an amide that has potent antitumor activity. It is a selective inhibitor of the protein kinase Raf (Akt), leading to inhibition of the growth of cancer cells in vitro. 2-Fluoro-4-nitrophenol also inhibits the proliferation of prostate cancer cells, which may be due to its ability to inhibit the production of growth factors and cytokines such as mcf-7 and nitrous oxide. The 2-fluoro-4-nitrophenol is cytotoxic because it inhibits DNA synthesis and prevents mitosis. The chemical structure consists of a nitro group (-NO2) on C6, a phenolic hydroxyl group (-OH) on C2, and a methylene group (-CH2-) on C3. This molecule binds covalently to proteins through its amino acid side chain at C6 and forms stable complexes with x-ray crystallography structures. It</p>

<p>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.</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>2-Aminobenzyl alcohol is a chaperone that binds to the polypeptide chain of proteins and prevents them from denaturation. It also has been shown to form hydrogen bonds with other molecules, such as chaperones, and to bind to copper ions. 2-Aminobenzyl alcohol can react with sodium carbonate in an alkaline solution to form 2-aminobenzaldehyde and sodium bicarbonate. The reaction mechanism is thought to involve the formation of a copper complex with x-ray diffraction data showing a new set of peaks at d = 1.81 Å corresponding to the Cu(II) ion coordinated by two amine groups on the benzyl alcohol ring. This compound also reacts with quinoline derivatives in the presence of hydrochloric acid or hydroxyl group in an aprotic solvent such as dimethylformamide (DMF) or acetonitrile (ACN) to produce mianserin hydro</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>Standard for determination of toxic monomers from polymer coatings</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>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>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>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>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>2,3-Difluoro-6-nitrophenol is a fluorinated phenolic compound that is used in biochemical research as a competitive inhibitor of bacterial growth. It is synthesized by the reaction of 2,3-difluorophenol with nitric acid. The chemical structure can be determined through infrared, NMR, and mass spectrometry techniques. 2,3-Difluoro-6-nitrophenol has been shown to inhibit bacterial growth by binding to the enzyme cytochrome c oxidase. This inhibition prevents electron transport from occurring, resulting in an accumulation of reactive oxygen species and cell death.</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>3-Hydroxy-4-methoxybenzyl alcohol is a metabolite of vanillic acid, an aldehyde that is produced by the oxidation of catecholamines. This compound has been shown to inhibit the activity of aldehyde oxidase, which converts aldehydes into acids. 3-Hydroxy-4-methoxybenzyl alcohol has also been shown to inhibit cellular dehydrogenase and protocatechuic aldehyde dehydrogenase activities, as well as inhibiting cellular metabolism.</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-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</p>

<p>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.</p>

<p>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.</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>2-Bromo-4,5-dimethoxybenzyl alcohol is an electrophilic brominating agent. It has been used in the synthesis of aryllithiums, organoiron compounds and chromenes. It is also used in the synthesis of nucleophiles, synthons and amaryllidaceae alkaloids. 2-Bromo-4,5-dimethoxybenzyl alcohol reacts with lithium diisopropylamide (LDA) to produce an aryllithium compound that is used as a nucleophile in organic synthesis reactions. This alcohol can be converted to an arene by reaction with carbon monoxide gas.</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>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>

<p>4-Acetamidophenol (4AP) is a natural compound that has been shown to inhibit nuclear DNA damage in vitro. It also has anti-inflammatory activity, which may be due to its ability to inhibit cyclooxygenase-1 and cyclooxygenase-2 enzymes. 4AP is synthesized by the condensation of acetaminophen with formaldehyde and sodium hydroxide. This drug binds to the signal peptide in the Toll-like receptor 2 (TLR2) protein, preventing TLR2 from activating inflammatory pathways. The matrix effect of 4AP is thought to play a role in its mechanism of action, as well as its biocompatibility with tissues.<br>The analytical method used for this product is high performance liquid chromatography with ultraviolet detection at 280 nm.</p>

<p>5-Bromo-2-hydroxybenzyl alcohol (5-BrABA) is a diagnostic agent that is used to detect microbial infections. It has been shown to be useful as an anti-infective agent in the treatment of cancer and inflammatory diseases, such as choroidal neovascularization. 5-BrABA is a cell permeable compound that binds to target tissue and accumulates at the site of infection. It has been shown to inhibit the growth of ophthalmic bacteria, including Acinetobacter baumannii, Pseudomonas aeruginosa, and Staphylococcus epidermidis. 5-BrABA has also been shown to be biocompatible with human retinal pigment epithelial cells and does not induce any detectable toxicity or cytotoxicity in these cells after 24 hours exposure.</p>

<p>4-Methylbenzyl alcohol is a reactive molecule that has been shown to form an acid in water. The formation of this acid can be attributed to the loss of a proton from the methyl group. This acid is generated by a reaction mechanism that involves the nucleophilic attack of hydrogen fluoride on the methyl group, leading to its conversion into a carbocation. 4-Methylbenzyl alcohol can also react with β-amino acids and hydrogen fluoride in organic solvents at high pH values, through similar mechanisms.</p>

<p>An enhancer used in chemiluminescent reactions</p>

<p>Component of polymer coatings in food cans; toxic contaminant</p>

<p>Chlorophenol red is a fluorescent probe that can be used in the detection of microbial infection. It has been shown to react with malonic acid (MAA) and fluoresce at an excitation wavelength of ~480 nm and emission wavelength of ~520 nm. The linear calibration curve for this assay was generated using human serum, which is a good model system for detecting infectious diseases. Chlorophenol red was also shown to bind to the receptor activity on mammalian cells and can be used as a marker for autoimmune diseases.</p>

<p>Substrate for acetyl esterase</p>

<p>4-Allyl-2-methoxyphenol acetate is a natural compound that has been shown to have inhibitory properties against Candida glabrata. It also has a synergistic effect with benzoate and eugenol, which are compounds that are found in the essential oils of plants. 4-Allyl-2-methoxyphenol acetate is toxic to aquatic organisms at high concentrations. The water solubility of this compound is low and it has a vapor pressure of 0.0045 mm Hg at 25°C, indicating that it will not evaporate into the atmosphere very quickly.</p>