|Related Categories||Carbohydrate Chemistry, Carbohydrate Derivatives, Chemical Biology, Chemical Synthesis|
|optical activity||[α]20/D +8.6°, c = 1.5% in chloroform|
|[α]24/D +23°, c = 1 in chloroform|
25, 100 g in glass bottle
Comparative structural analysis of 5,6,7,9-tetra-O-acetyl-4,8-anhydro-1,3-dideoxy-D-glycero-L-gluco-nonulose and its 1-O-acetylated analog, 1,2,3,4,6-penta-O-acetyl-beta-D-galactopyranose using X-ray crystallography. Kumar R, Tiwari P, Maulik PR, et al. Carbohydr. Res. 340(14), 2335-9, (2005)
Crystal structure of penta-O-acetyl-beta-D-galactopyranose with modeling of the conformation of the acetate groups. Thibodeaux DP, Johnson GP, Stevens ED, et al. Carbohydr. Res. 337(21-23), 2301-10, (2002)
Zeolite-catalyzed Helferich-type glycosylation of long-chain alcohols. Synthesis of acetylated alkyl 1,2-trans glycopyranosides and alkyl 1,2-cis C2-hydroxy-glycopyranosides. Aich U and Loganathan D Carbohydr. Res. 342(5), 704-9, (2007)
FT-NMR 1 (1), 1056:C / IR-Spectra (2), 330:G / IR-Spectra (3), 372:A / RegBook 1 (1), 761:N / Structure Index 1, 118:A:5
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