1383687-52-2

Basic information

• Product Name: 6-[[(propylamino)carbonyl]oxy]-1,3,2',6'-tetraazidoneamine
• CAS NO: 1383687-52-2
• Molecular Weight: 511.457
• Mol File: 1383687-52-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-[[(propylamino)carbonyl]oxy]-1,3,2',6'-tetraazidoneamine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-[[(propylamino)carbonyl]oxy]-1,3,2',6'-tetraazidoneamine(1383687-52-2)
• EPA Substance Registry System: 6-[[(propylamino)carbonyl]oxy]-1,3,2',6'-tetraazidoneamine(1383687-52-2)

Safety Data

• Hazardous Substances Data: 1383687-52-2(Hazardous Substances Data)

Upstream product

• 688744-66-3 1,3,2',6'-tetraazido-3',4'-di-O-acetylneamine 
• 182554-04-7 1,3,2′,6′-tetraazido-6,3′,4′-tri-O-acetylneamine 
• 671809-10-2 1,3,2′,6′-tetraazidoneamine 
• 3947-65-7 neomycin A 
• 107-10-8 propylamine 
• 1383687-47-5 5,6-[carbonylbis(oxy)]-3',4'-di-O-acetyl-1,3,2',6'-tetraazidoneamine 

Relevant articles and documents

Synthesis and antibacterial activity of novel neamine derivatives: Preponderant role of the substituent position on the neamine core

A series of neamine derivatives were prepared from the cyclic carbonate and sulfate of 1,3,2′,6′-tetraazido-3′,4′,-di-O- acetylneamine. Ring opening reactions with diversely substituted amines result in the formation of the corresponding carbamates or sulfonic acids with good overall yields. The antibacterial activities of the synthesized products against E. coli (DH5α) and S. aureus (RN4220) were evaluated. With isolated single regioisomers, the preponderant effect of the 5-positions of the carbamate substituent on the neamine core was demonstrated.