78216-83-8

Basic information

• Product Name: methyl 2-acetylamido-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside
• Synonyms: methyl 2-acetylamido-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside
• CAS NO: 78216-83-8
• Molecular Weight: 323.346
• Mol File: 78216-83-8.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: methyl 2-acetylamido-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-acetylamido-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside(78216-83-8)
• EPA Substance Registry System: methyl 2-acetylamido-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside(78216-83-8)

Safety Data

• Hazardous Substances Data: 78216-83-8(Hazardous Substances Data)

Upstream product

• 3055-46-7 methyl N-acetyl-D-glucosamine 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 128657-58-9 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 108-24-7 acetic anhydride 
• 6082-04-8 methyl 2-acetylamido-2-deoxy-D-glucoside 
• 100638-83-3 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O--α-D-glucopyranoside 
• 6619-02-9 methyl N-acetyl-2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 4288-74-8 methyl 2-N-acetylamido-4,6-O-benzylidene-2-deoxy-3-ulose-α-D-ribo-hexapyranoside 
• 67-56-1 methanol 
• 6748-94-3 methyl-[O³-acetyl-2-acetylamino-O⁴,O⁶-((R)-benzylidene)-2-deoxy-α-D-altropyranoside] 
• 66537-92-6 methyl 2,3-anhydro-4,6-benzylidene-α-D-allopyranoside 
• 7512-17-6 N-Acetyl-D-glucosamine 

Downstream Products

• 354986-48-4 methyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-(2-picolinyl)-α-D-glucopyranoside 
• 651736-01-5 methyl 2-amino-4,6-O-benzylidene-2-deoxy-α-D-allopyranoside 

Relevant articles and documents

Ultrasonication-Assisted Synthesis of a d-Glucosamine-Based β-CD Inclusion Complex and Its Application as an Aqueous Heterogeneous Organocatalytic System

For the first time, an inclusion complex has been crafted between a carbohydrate-based molecule and a β-cyclodextrin (CD) hydrophobic cavity for asymmetric catalytic applications. This novel d-glucosamine-based inclusion compound has been synthesized in h

D-Glucosamine as a novel chiral auxiliary for the stereoselective synthesis of P-stereogenic phosphine oxides

D-Glucosamine was successfully employed as a chiral auxiliary for the enantioselective synthesis of phosphine oxides. The influence of the anomeric position was also investigated and revealed the excellent ability of the α-anomer to perform this transform

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