5531-53-3

Basic information

• Product Name: 1-O,2-O,3-O,5-O,6-O-Pentaacetyl-β-D-galactofuranose
• Synonyms: 1-O,2-O,3-O,5-O,6-O-Pentaacetyl-β-D-galactofuranose;β-D-Galactofuranose pentaacetate
• CAS NO: 5531-53-3
• Molecular Formula: C₁₆H₂₂O₁₁
• Molecular Weight: 390.33928
• Mol File: 5531-53-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-O,2-O,3-O,5-O,6-O-Pentaacetyl-β-D-galactofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O,2-O,3-O,5-O,6-O-Pentaacetyl-β-D-galactofuranose(5531-53-3)
• EPA Substance Registry System: 1-O,2-O,3-O,5-O,6-O-Pentaacetyl-β-D-galactofuranose(5531-53-3)

Safety Data

• Hazardous Substances Data: 5531-53-3(Hazardous Substances Data)

Upstream product

• 59-23-4 D-Galactose 
• 108-24-7 acetic anhydride 
• 4451-36-9 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl chloride 
• 64-19-7 acetic acid 
• 543-80-6 barium(II) acetate 
• 563-63-3 silver(I) acetate 
• 10257-28-0 D-Galactose 

Downstream Products

• 1296128-99-8 N-benzoyl-α-D-galactofuranosylamide 
• 1277171-87-5 benzyl 2,3,5,6-tetra-O-acetyl-1-thio-β-D-galactofuranoside 
• 4671-52-7 N-benzyloxycarbonyl-O-(2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl)-L-serinyl methyl ester 
• 97321-48-7 4-O-acetyl-1,2,5,6-tetra-O-benzoyl-3-O-(2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl)-D-mannitol 
• 4144-97-2 O³-β-D-galactofuranosyl-D-mannitol 
• 107724-09-4 Allyl 2,3,6-tri-O-benzyl-5-O-(2,3,5,6-tetra-O-benzyl-β-D-galactofuranosyl)-β-D-galactofuranosid 
• 107691-65-6 Allyl 2,3,6-tri-O-benzyl-5-O-(2,3,5,6-tetra-O-acetyl-β-D-galactofuranosyl)-β-D-galactofuranoside 
• 107691-66-7 Allyl 2,3,6-tri-O-benzyl-5-O-β-D-galactofuranosyl-β-D-galactofuranoside 
• 107691-63-4 Allyl 2,3,6-tri-O-benzyl-β-D-galactofuranoside 
• 107691-61-2 Allyl 2,3-O-dibenzyl-5,6-O-isopropyliden-β-D-galactofuranoside 
• 107691-62-3 Allyl 2,3-O-dibenzyl-β-D-galactofuranoside 

Relevant articles and documents

Synthesis of immunostimulatory α- C -galactosylceramide glycolipids via sonogashira coupling, asymmetric epoxidation, and trichloroacetimidate- mediated epoxide opening

Stereocontrolled syntheses of α-C-GalCer (2) and its α-C-acetylenic analogue 6 were accomplished in high efficiency by a convergent construction strategy from 1-hexadecene and d-galactose. The key transformations include Sonogashira coupling, Sharpless asymmetric epoxidation, and Et2AlCl-catalyzed cyclization of an epoxytrichloroacetimidate to generate protected dihydrooxazine 21.

H-Beta zeolite as an efficient catalyst for per-O-acetylation of mono- and disaccharides

Among the six different zeolites examined, H-beta is demonstrated to be a highly efficient and selective catalyst for the per-O-acetylation of various mono-and disaccharides and methyl glycosides.