549501-26-0

Basic information

• Product Name: 5,6-di-O-acetyl-3',4'-di-O-benzyl-1,3,2',3'-tetraazidoneamine
• Synonyms: 5,6-di-O-acetyl-3',4'-di-O-benzyl-1,3,2',3'-tetraazidoneamine
• CAS NO: 549501-26-0
• Molecular Weight: 690.676
• Mol File: 549501-26-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5,6-di-O-acetyl-3',4'-di-O-benzyl-1,3,2',3'-tetraazidoneamine(CAS DataBase Reference)
• NIST Chemistry Reference: 5,6-di-O-acetyl-3',4'-di-O-benzyl-1,3,2',3'-tetraazidoneamine(549501-26-0)
• EPA Substance Registry System: 5,6-di-O-acetyl-3',4'-di-O-benzyl-1,3,2',3'-tetraazidoneamine(549501-26-0)

Safety Data

• Hazardous Substances Data: 549501-26-0(Hazardous Substances Data)

Upstream product

• 632330-84-8 phenyl 2,6-diazido-2,6-dideoxy-1-thio-α/β-D-glucopyranoside 
• 632330-83-7 Toluene-4-sulfonic acid (2R,3S,4R,5R)-5-azido-3,4-dihydroxy-6-phenylsulfanyl-tetrahydro-pyran-2-ylmethyl ester 
• 183875-22-1 phenyl 2-azido-2-deoxy-3,4,6-tri-O-acetyl-1-thio-α/β-D-glucopyranoside 
• 202462-37-1 phenyl 2-azido-2-deoxy-1-thio-α/β-D-glucopyranoside 
• 171032-74-9 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-D-glucopyranose 
• 688744-65-2 1,3,2’,6’-tetrazido-5,6-O-cyclohexylidene neamine 
• 100-39-0 benzyl bromide 
• 75-36-5 acetyl chloride 
• 549501-27-1 3′,4′-di-O-benzyl-1,3,2′,6′-tetraazidoneamine 
• 236115-61-0 [(1S,2S,3R,4S,6R)-2-acetoxy-4,6-diazido-3-hydroxy-cyclohexyl] acetate 
• 549501-23-7 (3R,4R,5R,6R)-3-Azido-6-azidomethyl-4,5-bis-benzyloxy-2-phenylsulfanyl-tetrahydro-pyran 

Downstream Products

• 549501-35-1 (1S,2R,3R,4S,6R)-4,6-Diamino-3-((2R,3R,4R,5R,6R)-3-amino-6-aminomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-cyclohexane-1,2-diol 
• 3947-65-7 neomycin A 
• 549501-27-1 3′,4′-di-O-benzyl-1,3,2′,6′-tetraazidoneamine 

Relevant articles and documents

Tuning the regioselectivity of the staudinger reaction for the facile synthesis of kanamycin and neomycin class antibiotics with N-1 modification

(Chemical Equation Presented) A novel method for achieving the desired regioselective reduction of the N-1 azido group on a tetraazidoneamine has been developed that leads to the synthesis of both kanamycin and neomycin class antibiotics bearing N-1 modif