1370586-85-8

Basic information

• Product Name: methyl 2-acetamido-4,6-di-O-benzoyl-2-deoxy-α-D-ribo-hexapyranoside-3-ulose
• Synonyms: methyl 2-acetamido-4,6-di-O-benzoyl-2-deoxy-α-D-ribo-hexapyranoside-3-ulose
• CAS NO: 1370586-85-8
• Molecular Weight: 441.438
• Mol File: 1370586-85-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-acetamido-4,6-di-O-benzoyl-2-deoxy-α-D-ribo-hexapyranoside-3-ulose(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-acetamido-4,6-di-O-benzoyl-2-deoxy-α-D-ribo-hexapyranoside-3-ulose(1370586-85-8)
• EPA Substance Registry System: methyl 2-acetamido-4,6-di-O-benzoyl-2-deoxy-α-D-ribo-hexapyranoside-3-ulose(1370586-85-8)

Safety Data

• Hazardous Substances Data: 1370586-85-8(Hazardous Substances Data)

Upstream product

• 6082-04-8 methyl 2-acetylamido-2-deoxy-D-glucoside 
• 98-88-4 benzoyl chloride 
• 4288-74-8 methyl 2-N-acetylamido-4,6-O-benzylidene-2-deoxy-3-ulose-α-D-ribo-hexapyranoside 
• 1125-88-8 benzaldehyde dimethyl acetal 

Relevant articles and documents

3- and 4-uloses derived from N-acetyl- D -glucosamine: A unique pair of complementary organocatalysts for asymmetric epoxidation of alkenes

The 4-ulose and the 3-ulose, both derived in two steps from the α-methyl glycoside of N-acetyl-D-glucosamine (GlcNAc), act as organocatalysts in the asymmetric epoxidation of alkenes, with unprecedented complementary enantioselectivity. The best results are found with α,β-unsaturated esters as substrates, with enantiomeric ratios up to 90:10 and 11:89, respectively. Copyright