251086-00-7

Basic information

• Product Name: (2S,4R)-2-[(R)-((2S,3R,4R,5S,6R)-5-Benzyloxy-4-hydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-hydroxy-methyl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester
• Synonyms: (2S,4R)-2-[(R)-((2S,3R,4R,5S,6R)-5-Benzyloxy-4-hydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-hydroxy-methyl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester
• CAS NO: 251086-00-7
• Molecular Weight: 483.559
• Mol File: 251086-00-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,4R)-2-[(R)-((2S,3R,4R,5S,6R)-5-Benzyloxy-4-hydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-hydroxy-methyl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4R)-2-[(R)-((2S,3R,4R,5S,6R)-5-Benzyloxy-4-hydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-hydroxy-methyl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester(251086-00-7)
• EPA Substance Registry System: (2S,4R)-2-[(R)-((2S,3R,4R,5S,6R)-5-Benzyloxy-4-hydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-hydroxy-methyl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester(251086-00-7)

Safety Data

• Hazardous Substances Data: 251086-00-7(Hazardous Substances Data)

Upstream product

• 100-51-6 benzyl alcohol 
• 251085-96-8 (2S,4R)-2-[(R)-((1R,2S,5R)-2-Benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-3-en-4-yl)-hydroxy-methyl]-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 251085-95-7 Trifluoro-methanesulfonic acid (1R,2S,5R)-2-benzyloxy-6,8-dioxa-bicyclo[3.2.1]oct-3-en-4-yl ester 
• 102719-10-8 1,6-anhydro-4-O-benzyl-3-deoxy-β-D-erythro-hexopyranos-2-ulose 
• 37112-31-5 levoglucosenone 
• 251085-99-1 (2S,4R)-2-[(R)-((2S,5S,6R)-5-Benzyloxy-6-hydroxymethyl-2-methoxy-5,6-dihydro-2H-pyran-3-yl)-hydroxy-methyl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

Convergent synthesis of (1→2)- and (1→4)-C-linked imino disaccharides

A convergent synthesis of (1→2)- and (1→4)-C-linked imino disaccharides was achieved by applying Nozaki-Kishi coupling of a hydroxyproline-derived carbaldehyde with isolevoglucosenone or levoglucosenone derived enol triflates.