Alcools benzyliques

Applications Benzyl-2,3,4,5,6-D5 Alcohol is an isotopically labeled analog of Benzyl Alcohol (T536635), which is used in the synthesis of Cephalosporolide B as a versatile biomimetic synthetic precursor for chemical synthesis of other cephalosporides.
References Song, L. et al.: Org. Lett., 15, 5850 (2013);

Stability Moisture Sensitive
Applications 4-Chlorobenzyl Chloride is a benzylchloride derivative used in the preparation of various biologically active compounds such as bronchodilators and antibacterial agents.
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 Adams, M. et al.: Synth. Comm., 29, 2419 (1999); Foroumadi, A. et al.: Arch. Pharm. Res., 30, 138 (2007);

单酚香气;胶粘剂;密封剂;抗氧化剂;消毒剂

5-Amino-2-methoxyphenol is a p-hydroxybenzoic acid, which is an amide derivative of 5-amino-2-methoxybenzoic acid. It can be used to prepare a sample for the detection of fatty acids in human serum by cycle analysis. 5-Amino-2-methoxyphenol has been shown to have antinociceptive properties and can be used as a chemical precursor in the synthesis of other compounds. The reaction mechanism for 5-Amino-2-methoxyphenol has been determined using NMR spectroscopy and chemical structures. The compound is stable at neutral pH and reacts with hydrogen to form an intramolecular hydrogen bond between the hydroxyl group and the nitrogen atom on the amino group.

Synthetic building block; biomimetic anti-fungal

3-Aminobenzyl alcohol is a prodrug that is metabolized to 3-aminophenol, its active form. It has immunomodulatory properties and can be used to treat population growth. 3-Aminobenzyl alcohol binds to specific receptors on the surface of lymphocytes, which inhibits the immune system's response to foreign antigens. This drug also has photochemical properties and can be used as a photosensitizer in photodynamic therapy. 3-Aminobenzyl alcohol is a hydrogen bond acceptor with acidic functional groups and has been shown to bind with proteins through hydrogen bonding interactions. The hydrogen bond strength between the drug and protein depends on the pH of the solution, which may affect its efficacy in different cell types.

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3-Phenoxybenzyl alcohol is a chemical compound that has a basic structure. It is soluble in water and organic solvents, but not in hydrochloric acid. This compound is used as an intermediate to produce other chemicals. 3-Phenoxybenzyl alcohol has been shown to inhibit the growth of bacteria by preventing the formation of fatty acids during the metabolism process. The production of epidermal growth factor and acid formation were inhibited by 3-phenoxybenzyl alcohol in rat liver microsomes. Recombinant cytochrome P450 enzymes have also been shown to be inhibited by this compound, which may lead to analytical methods for determining its concentration in blood plasma or urine.

2-Bromo-4-iodobenzyl alcohol is a versatile building block that can be used in the synthesis of complex compounds. It is a high quality, useful intermediate that can be used as a reaction component or scaffold for the synthesis of many different compounds. This chemical is also useful for research purposes and as a reagent.

3-Iodobenzyl alcohol is a pesticide that belongs to the class of halogenated benzaldehydes. It is a bioconjugate, which means that it can be coupled to an organic molecule to form a new molecule with improved properties. 3-Iodobenzyl alcohol is used in the synthesis of polymers and pharmaceuticals. In addition, 3-iodobenzyl alcohol has been studied as an anticancer drug candidate because it binds to DNA and inhibits DNA synthesis and repair in tumor cells. This compound has also been shown to be effective against methicillin resistant Staphylococcus aureus (MRSA) isolates.

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3,5-Diaminobenzyl alcohol dihydrochloride is a quinoline derivative that is cytotoxic to tumor cells. It binds to the DNA and inhibits protein synthesis by inhibiting the enzyme ribonucleotide reductase. 3,5-Diaminobenzyl alcohol dihydrochloride has been shown to be cytotoxic in the nanomolar range against tumor cells and is an antitumor agent. This drug has been shown to inhibit growth of cells in culture by binding to DNA.

4-Amino-2-nitrophenol (4ANP) is a chemical substance that has been shown to be carcinogenic in animal models. It has also been shown to induce bladder cancer in women who are occupationally exposed to the chemical. The carcinogenic potential of 4ANP is due to its ability to react with nucleophilic groups such as amines and hydroxyl groups on proteins, DNA, and RNA. This reaction leads to the formation of nitrosamines and their metabolites, which are known carcinogens. 4ANP can also act as a receptor molecule for certain types of cancer cells. These interactions have been studied using chromatographic methods.