114040-93-6

Basic information

• Product Name: 2-acetamido-N-benzyl-3-O-benzyl-1,2,5-trideoxy-1,5-imino-4,6-O-isopropylidene-D-glucitol
• CAS NO: 114040-93-6
• Molecular Weight: 424.54
• Mol File: 114040-93-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-acetamido-N-benzyl-3-O-benzyl-1,2,5-trideoxy-1,5-imino-4,6-O-isopropylidene-D-glucitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-acetamido-N-benzyl-3-O-benzyl-1,2,5-trideoxy-1,5-imino-4,6-O-isopropylidene-D-glucitol(114040-93-6)
• EPA Substance Registry System: 2-acetamido-N-benzyl-3-O-benzyl-1,2,5-trideoxy-1,5-imino-4,6-O-isopropylidene-D-glucitol(114040-93-6)

Safety Data

• Hazardous Substances Data: 114040-93-6(Hazardous Substances Data)

Upstream product

• 114040-86-7 N-benzyl-1,5-dideoxy-1,5-imino-4,6-O-isopropylidene-D-glucitol 
• 114040-88-9 N-benzyl-1,2,3,5-tetradeoxy-1,5-imino-4,6-O-isopropylidene-D-erythro-2-hexenitol 
• 72458-46-9 N-benzyl-1-deoxynojirimycin 
• 19130-96-2 1,5-dideoxy-1,5-imino-D-glucitol 
• 108-24-7 acetic anhydride 
• 114040-92-5 (4aR,7S,8R,8aR)-5-Benzyl-8-benzyloxy-2,2-dimethyl-hexahydro-[1,3]dioxino[5,4-b]pyridin-7-ylamine 
• 100-39-0 benzyl bromide 
• 114040-90-3 N-benzyl-3-O-benzyl-1,5-dideoxy-1,5-imino-4,6-O-isopropylidene-2-O-(trifluoro-methyl)sulfonyl-D-mannitol 
• 114040-87-8 N-benzyl-1,5-dideoxy-1,5-imino-4,6-O-isopropylidene-2,3-di-O-(methylsulfonyl)-D-glucitol 
• 114040-91-4 2-azido-N-benzyl-3-O-benzyl-1,2,5-trideoxy-1,5-imino-4,6-O-isopropylidene-D-glucitol 
• 114040-89-0 N-benzyl-3-O-benzyl-1,5-dideoxy-1,5-imino-4,6-O-isopropylidene-D-mannitol 
• 114129-23-6 N-benzyl-1,5-dideoxy-1,5-imino-4,6-O-isopropylidene-D-mannitol 

Downstream Products

• 105265-96-1 2-acetamido-1,2-dideoxynojirimycin 

Relevant articles and documents

The chemistry of the 1-deoxynojirimycin system. Synthesis of 2-acetamido-1,2-dideoxynojirimycin from 1-deoxynojirimycin.

The synthesis of 2-acetamido-1,2-dideoxynojirimycin (2-acetamido-1,2,5-tri-deoxy-1,5-imino-D-glucitol) by a double inversion procedure starting from 1-deoxynojirimycin is reported. The key intermediates were the selectively protected N-benzyl-1,5-dideoxy-