381724-74-9

Basic information

• Product Name: ((3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester
• Synonyms: ((3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester
• CAS NO: 381724-74-9
• Molecular Weight: 654.8
• Mol File: 381724-74-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: ((3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester(381724-74-9)
• EPA Substance Registry System: ((3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid tert-butyl ester(381724-74-9)

Safety Data

• Hazardous Substances Data: 381724-74-9(Hazardous Substances Data)

Upstream product

• 150942-98-6 t-butyl lithioacetate 
• 82598-84-3 2,3,4,6-tetra-O-benzyl-D-galactonolactone 

Downstream Products

• 381724-80-7 N-[(2S,3R,4S,5S,6R)-2-(Benzylcarbamoyl-methyl)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl]-benzamide 
• 381724-76-1 (6S,8R,9S,10S,11R)-9,10,11-Tris-benzyloxy-8-benzyloxymethyl-2-phenyl-3,7-dioxa-1-aza-spiro[5.5]undec-1-en-4-one 
• 849472-56-6 (S)-t-butyl 4-(2-((2S,3R,4S,5S,6R)-2-benzamido-3,4,5-tris(benzyloxy)-6-benzyloxymethyltetrahydro-2H-pyran-2-yl)acetamido)-2-(t-butoxycarbonylamino)butanoate 
• 849472-65-7 (S)-4-(2-((2S,3R,4S,5R,6R)-2-benzamido-3,4,5-tris(acetoxy)-6-acetoxymethyltetrahydro-2H-pyran-2-yl)acetamido)-2-(9-fluorenylmethoxycarbonylamino)butanoic acid 
• 849472-72-6 (S)-2-tert-Butoxycarbonylamino-4-[2-((2S,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-2-benzoylamino-tetrahydro-pyran-2-yl)-acetylamino]-butyric acid tert-butyl ester 
• 381724-75-0 ((3R,4S,5S,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-hydroxy-tetrahydro-pyran-2-yl)-acetic acid 

Relevant articles and documents

One pot conversion of ketoses into sugar β-peptides via a ritter reaction

α-D-Galacto-2-deoxy-oct-3-ulopyranosonic acids can be converted into unnatural glycopeptides via a one pot intramolecular Ritter reaction. Initially, the ketopyranoside reacts under Lewis acid catalyzed conditions with a nitrile (aromatic or aliphatic) to