1422740-11-1

Basic information

• Product Name: C₃₃H₅₁NO₆Si
• CAS NO: 1422740-11-1
• Molecular Weight: 585.857
• Mol File: 1422740-11-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₃H₅₁NO₆Si(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₃H₅₁NO₆Si(1422740-11-1)
• EPA Substance Registry System: C₃₃H₅₁NO₆Si(1422740-11-1)

Safety Data

• Hazardous Substances Data: 1422740-11-1(Hazardous Substances Data)

Upstream product

• 1422740-12-2 C₁₉H₃₇NO₄Si 
• 1422740-10-0 C₁₃H₂₅NO₆ 
• 130532-54-6 (S)-((1E)-3-hydroxy-propenyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 129483-65-4 (4S)-1,1-Dimethylethyl 4-<(E)-3'-methoxy-3'-oxo-1'-propenyl>-2,2-dimethyl-3-oxazolidinecarboxylate 
• 126587-35-7 methyl (4S)-4-[(tert-butoxy)carbonylamino]-5-hydroxypentanoate 
• 81658-26-6 tert-butyl (S)-2-(((tert-butyldimethylsilyl)oxy)methyl)-5-oxopyrrolidin-1-carboxylate 
• 136904-77-3 (4S)-4-(2-methoxycarbonylethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 96014-55-0 Methyl (4S)-4-(N-(tert-Butoxycarbonyl)amino)-5-((tert-butyldimethylsilyl)oxy)pentanoate 
• 1422740-16-6 C₁₉H₃₉NO₆Si 
• 100-39-0 benzyl bromide 

Relevant articles and documents

New approach toward the total synthesis of (+)-batzellaside B

A new synthetic approach to (+)-batzellaside B from naturally abundant L-pyroglutamic acid is presented in this article. The key synthetic step involves Sharpless asymmetric dihydroxylation of an olefinic substrate functionalized with an acetoxy group to