18981-64-1

Basic information

• Product Name: methyl 2,3,6-trideoxy-3-triaza-1,2-dien-2-ium-1-ylhexopyranoside
• CAS NO: 18981-64-1
• Molecular Formula: C₇H₁₄N₃O₃
• Molecular Weight: 188.2038
• Mol File: 18981-64-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 2,3,6-trideoxy-3-triaza-1,2-dien-2-ium-1-ylhexopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2,3,6-trideoxy-3-triaza-1,2-dien-2-ium-1-ylhexopyranoside(18981-64-1)
• EPA Substance Registry System: methyl 2,3,6-trideoxy-3-triaza-1,2-dien-2-ium-1-ylhexopyranoside(18981-64-1)

Safety Data

• Hazardous Substances Data: 18981-64-1(Hazardous Substances Data)

Upstream product

• 34819-86-8 3,4-di-O-acetyl-6-deoxy-L-glucal 
• 20770-58-5 Acetic acid (1S,2S)-2,3-diacetoxy-1-((S)-1,2-diacetoxy-ethyl)-4-nitro-butyl ester 
• 87782-52-3 Methyl 2-deoxy-α-L-arabino-hexopyranoside 6-p-toluenesulfonate 
• 87782-50-1 Methyl 2-deoxy-α-L-arabino-hexopyranoside 
• 87782-51-2 (2S,3R,4S,6S)-2-Hydroxymethyl-6-methoxy-tetrahydro-pyran-3,4-diol 
• 3971-45-7 (2S,3R,4S)-2-Hydroxymethyl-6-methoxy-tetrahydro-pyran-3,4-diol 
• 23568-30-1 2-Deoxy-L-arabino-hexose 
• 87782-56-7 Methyl 2-deoxy-α-L-arabino-hexopyranoside 3,4,6-tri-p-toluenesulfonate 
• 87782-55-6 Methyl 2-deoxy-α-L-arabino-hexopyranoside 3,6-di-p-toluenesulfonate 
• 87858-15-9 3,4,5,6-Tetra-O-acetyl-1,2-dideoxy-1-nitro-L-arabino-hexitol 
• 18981-62-9 methyl 3-azido-2,3,6-trideoxy-4-O-methanesulphonyl-α-L-arabino-hexopyranoside 
• 87782-54-5 Methyl 2,6-dideoxy-6-iodo-α-L-arabino-hexopyranoside 
• 87858-14-8 3,4,5,6-Tetra-O-acetyl-1,2-dideoxy-1-nitro-L-arabino-hex-1-enitol 
• 18981-61-8 Methyl 2,6-dideoxy-α-L-arabino-hexopyranoside 3-p-toluenesulfonate 

Downstream Products

• 18977-92-9 methyl α-L-daunosaminide 

Relevant articles and documents

Addition of Hydrazoique Acid to Pseudoglycals Stereoselective Synthesis of L-Acosamine and L-Daunosamine

Methyl and benzyl glycosides and glycal of L-acosamine (3-amino-2,3,6 trideoxy-L-arabino-hexose) have been stereoselectively prepared via 1,4-addition of hydrazoic acid to L-erythro-hex-2-enopyranose as a key step.Inversion of the C-4 configuration of met