937021-95-9

Basic information

• Product Name: (2R,3R,4R,5R,6R)-3-azido-6-(azidomethyl)-4,5-bis(benzyloxy)-2-(((1R,2R,3S,4R,6S)-4,6-diazido-2,3-bis(benzyloxy)cyclohexyl)oxy)tetrahydro-2H-pyran
• Synonyms: (2R,3R,4R,5R,6R)-3-azido-6-(azidomethyl)-4,5-bis(benzyloxy)-2-(((1R,2R,3S,4R,6S)-4,6-diazido-2,3-bis(benzyloxy)cyclohexyl)oxy)tetrahydro-2H-pyran
• CAS NO: 937021-95-9
• Molecular Weight: 786.85
• Mol File: 937021-95-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,3R,4R,5R,6R)-3-azido-6-(azidomethyl)-4,5-bis(benzyloxy)-2-(((1R,2R,3S,4R,6S)-4,6-diazido-2,3-bis(benzyloxy)cyclohexyl)oxy)tetrahydro-2H-pyran(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R,4R,5R,6R)-3-azido-6-(azidomethyl)-4,5-bis(benzyloxy)-2-(((1R,2R,3S,4R,6S)-4,6-diazido-2,3-bis(benzyloxy)cyclohexyl)oxy)tetrahydro-2H-pyran(937021-95-9)
• EPA Substance Registry System: (2R,3R,4R,5R,6R)-3-azido-6-(azidomethyl)-4,5-bis(benzyloxy)-2-(((1R,2R,3S,4R,6S)-4,6-diazido-2,3-bis(benzyloxy)cyclohexyl)oxy)tetrahydro-2H-pyran(937021-95-9)

Safety Data

• Hazardous Substances Data: 937021-95-9(Hazardous Substances Data)

Upstream product

• 15446-43-2 neamine tetrahydrochloride 
• 100-39-0 benzyl bromide 
• 671809-10-2 1,3,2′,6′-tetraazidoneamine 
• 1197981-91-1 C₂₇H₂₈N₆O₃S 
• 499195-32-3 1,3-di-azido-5,6-di-O-benzyl-2-deoxystreptamine 
• 25389-98-4 neomycin B sulphate 

Downstream Products

• 285994-75-4 (S)-1-[(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]-3-methylamino-propan-2-ol 
• 285994-77-6 (R)-1-[(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]-3-methylamino-propan-2-ol 

Relevant articles and documents

A short and scalable route to orthogonally O-protected 2-deoxystreptamine

(Chemical Equation Presented) A seven-step synthesis of orthogonally O-protected 2-deoxy-streptamine has been developed from readily available neomycin, with an overall yield of 28%. Key chemical transformations include a chemoselective glycosidic bond hy

Investigation of the regioselectivity for the Staudinger reaction and its application for the synthesis of aminoglycosides with N-1 modification

(Chemical Equation Presented) The criteria for controlling the regioselectivity of Staudinger reduction of azides have been investigated. These findings enable a convenient direct N-1 modification of the perazidoneamine and perazidoribostamycin resulting