Álcoois

Applications 2-(Octadecyloxy)Ethanol (cas# 2136-72-3) is a useful research chemical.

Applications trans-2-Butene-1,4-diol can be used as an extender in polyurethanes and as a catalyst precursor in the preparation of α,ω,kentro-telechelic poly(THF).
References Lin, I. Sioun, et al.: J. of Elastomers & Plastics, 16(4), 265-80 (1984); Oike, Hideaki, et al.: Macromol., 33(23), 8898-8903 (2000)

Applications 4-(tert-Butoxycarbonyloxy)benzylalcohol (cas# 156281-11-7) is a compound useful in organic synthesis.

Applications 1-Azido-3,6,9-trioxaundecane-11-ol (cas# 86770-67-4) is a compound useful in organic synthesis.
References Hatch, D., et al.: ChemBioChem., 9, 2433 (2008),

Applications 4-{[(p-Fluorophenyl)imino]methyl}phenol is used in the preparation of benzylacetones which promote anti-fungal activity.
References Sandhar, R. et al.: J. Ind. Council Chem., 22, 32 (2005);

Stability Dimerizes Readily - Store Under Inert Atmosphere
Applications 4-Mercaptobenzyl Alcohol, 90% (cas# 53339-53-0) is a compound useful in organic synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications 2-Butoxyethanol is a reagent in the synthesis of 4-butoxyethoxy-N-octadecyl-1,8-naphthalimide as a new fluorescent probe for the determination of proteins. Also used as a reagent in the synthesis of 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors.
References Sun, Y., et al.: Bioorg. Med. Chem. Lett., 21, 3798 (2011); Yi, W., et al.: Eur. J. Med. Chem., 45, 639 (2010)

Applications 1-(hydroxymethyl)cyclopentan-1-ol (cas# 74397-18-5) is a useful research chemical.

Applications 4-Pentyn-1-ol is an alkyne alcohol that is used as an initiator in ring-opening polymerization reactions. 4-Pentyn-1-ol is capable of undergoing cyclosisomerization, and is also used as a reactant in the synthesis of (+)-Serinolamide A, a cannabinoid CB1 receptor agonist.
References Gao, Y., et al.: Tetrahedron Lett., 54, 6511 (2013); Liao, R., et al.: Proc. Nat. Acad. Sci., 107, 22523 (2010); Miranda, P., et al.: Org. Lett., 5, 1979 (2003); Xu, N., et al.: Macromol. Chem. Phys., 208, 730 (2007)