Alcools

Applications Bromo-tert-butyl Alcohol, is an organic building block that can be used in the variety of chemical synthesis. It is used in the synthesis of Monohalogeno-t-butyloxycarbonylamino Acids.
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 Takanobu, O. et al.: Bull. Chem.Sco. Jap., 45, 2603 (1972);

Applications 4-Amino-2-isopropylphenol is a building block used in the preparation of benzoate and benzamide derivatives as FXR antagonists.
References Song, K., et al.: Bioorg. Med. Chem., 23, 6427 (2015);

Applications 4-​Bromo-​3-​methyl-2-buten-1-ol is an intermediate in the synthesis of 2-[(4-Bromo-3-methyl-2-buten-1-yl)oxy]tetrahydro-2H-pyran (B681855), which is a tetrahydropyran protected intermediate used in the synthesis of L-Cysteine derivatives.

Applications 4-(phenylsulfanyl)phenol (cas# 5633-55-6) is a useful research chemical.

Applications (S,S)-2,3-Butanediol is the (S,S)-isomer of 2,3-Butanediol (B690020), a naturally occurring compound found in cocoa butter.
References Wang, Yu., et al.: J. Biological. Chem., 289, 6080 (2014); Cheng, C., et al.: J. Org. Chem., 78, 8562 (2013);

Applications 2-(Tetrahydro-2H-pyran-3-yl)ethanol (cas# 1050493-77-0) is a useful research chemical.

Applications 1-Nonadecanol (cas# 1454-84-8) is a useful research chemical.

Stability Unstable in Solution, Air Sensitive
Applications 2-HYDROXYTHIOPHENOL (cas# 1121-24-0) is a useful research chemical.

Applications 3,5,5-Trimethyl-1-hexanol can be used as a fragrance material and a flavoring agent for food.
References McGinty, D., et al.: Food and Chem. Toxic., 48(Suppl. 4), S47-S50 (2010);Letizia, C. S., et al.: Food and Chem. Toxic., 38(Suppl. 3), S223-S225 (2000)

1H-Pyrazol-4-ol is a molecule that has been shown to have antibacterial properties by inhibiting the growth of bacteria. It was also found to be effective in inhibiting the activity of dopamine β-hydroxylase, which is an enzyme that catalyzes the conversion of dopamine to norepinephrine. 1H-Pyrazol-4-ol has been shown to inhibit nitrite ion reductase, which converts nitrite ions into nitric oxide. Nitric oxide is a potent vasodilator and can cause hypotension. 1H-Pyrazol-4-ol also inhibits the formation of nitro groups from diazonium salts, which are used in many industrial processes, including dyeing and photography. 1H-Pyrazol-4-ol is activated by UV light and reacts with epididymal adipose tissue (fatty tissue) in rats to generate pyrazole derivatives with cytotoxic effects on liver

4-Hydroxy-3-nitro-2(1H)-quinolinone is a quinoline derivative that has been shown to have anticancer activity against cancer cells. It can be used for the treatment of various types of cancer, including lung cancer, breast cancer, and colon cancer. This drug inhibits the growth of cancer cells by blocking the cycle at the G1 phase and inducing apoptosis. It also disrupts mitochondrial membrane potential, leading to an increase in reactive oxygen species and DNA damage. 4-Hydroxy-3-nitro-2(1H)-quinolinone is an epidermal growth factor receptor (EGFR) antagonist and blocks epidermal growth factor signaling through its inhibition of EGFR tyrosine kinase activity. It also downregulates TNFα expression in tumor cells by inhibiting NFκB activation.

Estra-1,3,5(10),6-tetraene-3,17-diol is a sulfonated derivative of estradiol. It is used as a ligand in binding assays to measure the affinity of various compounds for estrogens. Estra-1,3,5(10),6-tetraene-3,17-diol binds with high affinity to 17β-estradiol and other estrogens at the estrogen receptor. The binding of estradiol and its derivatives to the receptor leads to a conformational change that causes dissociation of heat shock proteins from the receptor. This results in an increase in transcriptional activity of the receptor and increased synthesis of mRNA.

(R)-1-Phenylethanol is an organic compound that belongs to the class of aldehydes. It has an optimal redox potential and is used as a reactive intermediate in surface methodology. The kinetic data for this compound have been reported, including its reaction solution, kinetic, and stereoselective properties. (R)-1-Phenylethanol can be used to synthesize aromatic hydrocarbons with acyl chains or amines, using enzymatic reactions. It can also be used as an asymmetric synthesis reagent for the preparation of chiral alcohols and amines.