30688-38-1

Basic information

• Product Name: N-[(2R,3R,4R,5S,6R)-2-(2-Benzyloxy-1-benzyloxymethyl-ethoxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl]-acetamide
• Synonyms: N-[(2R,3R,4R,5S,6R)-2-(2-Benzyloxy-1-benzyloxymethyl-ethoxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl]-acetamide
• CAS NO: 30688-38-1
• Molecular Weight: 475.539
• Mol File: 30688-38-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-[(2R,3R,4R,5S,6R)-2-(2-Benzyloxy-1-benzyloxymethyl-ethoxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl]-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(2R,3R,4R,5S,6R)-2-(2-Benzyloxy-1-benzyloxymethyl-ethoxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl]-acetamide(30688-38-1)
• EPA Substance Registry System: N-[(2R,3R,4R,5S,6R)-2-(2-Benzyloxy-1-benzyloxymethyl-ethoxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl]-acetamide(30688-38-1)

Safety Data

• Hazardous Substances Data: 30688-38-1(Hazardous Substances Data)

Upstream product

• 10378-06-0 2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline 
• 30688-37-0 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-tetrahydro-pyran-4-yl ester 
• 6972-79-8 dibenzyl glycerol 

Relevant articles and documents

Synthesis of glycosyl glycerols and related glycolipids

Several isomeric glycosyl glycerols were synthesized. Acetylated allyl glycosides of D-glucose and D-galactose were transformed into 1-O-(glycopyranosyl)-rac-glycerols in a three step procedure via the corresponding 2,3-epoxypropyl glycosides and the peracetylated glycosyl glycerols. Tetra-O-benzyl-D-glucose was glycosylated with 1,3-di-O-benzylglycerol to give the α-anomer preferentially. The 2-O-(tetra-O-acetyl-β-glycopyranosyl)-sn-glycerols and 2-O-(β-glycopyranosyl)-sn-glycerols of D-glucose, D-galactose and N-acetyl-D-glucosamine and the corresponding α-derivatives of D-mannose were synthesized by selective glycosylation methods from 1,3-di-O-benzylglycerol and 1,3-O-benzylideneglycerol, respectively, and activated sugar compounds followed by hydrogenolysis. After long chain acylation and selective deacetylation the 1,3-di-O-acyl-2-O-β-glycopyranosyl)-sn-glycerols of D-glucose, D-galactose and N-acetyl-D-glucosamine and the corresponding α-derivative of D-mannose were synthesized.