236115-88-1

Basic information

• Product Name: ((S)-5-{2-[(1R,2R,3S,5R,6S)-3,5-Diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-ethylamino}-6-hydroxy-hexyl)-carbamic acid benzyl ester
• Synonyms: ((S)-5-{2-[(1R,2R,3S,5R,6S)-3,5-Diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-ethylamino}-6-hydroxy-hexyl)-carbamic acid benzyl ester
• CAS NO: 236115-88-1
• Molecular Weight: 989.104
• Mol File: 236115-88-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((S)-5-{2-[(1R,2R,3S,5R,6S)-3,5-Diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-ethylamino}-6-hydroxy-hexyl)-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: ((S)-5-{2-[(1R,2R,3S,5R,6S)-3,5-Diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-ethylamino}-6-hydroxy-hexyl)-carbamic acid benzyl ester(236115-88-1)
• EPA Substance Registry System: ((S)-5-{2-[(1R,2R,3S,5R,6S)-3,5-Diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-ethylamino}-6-hydroxy-hexyl)-carbamic acid benzyl ester(236115-88-1)

Safety Data

• Hazardous Substances Data: 236115-88-1(Hazardous Substances Data)

Upstream product

• 236115-81-4 5-O-allyl-1,3,2',6'-tetraazido-6,3',4'-tri-O-benzyl neamine 
• 236115-80-3 1,3,2',6'-tetraazido-6,3',4'-tri-O-benzyl neamine 
• 101250-90-2 (S)-2-amino-6-(benzyloxycarbonylamino)-1-hexanol 
• 236115-82-5 [(1R,2R,3S,5R,6S)-3,5-Diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-acetaldehyde 

Relevant articles and documents

Design and synthesis of new aminoglycoside antibiotics containing neamine as an optimal core structure: Correlation of antibiotic activity with in vitro inhibition of translation

The structure and activity of the pseudodisaccharide core found in aminoglycoside antibiotics was probed with a series of synthetic analogues in which the position of amino groups was varied around the glucopyranose ring. The naturally occurring structure