153172-36-2

Basic information

• Product Name: (3aR,4R,6S,6aS)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-6-[2-phenylsulfanyl-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole
• CAS NO: 153172-36-2
• Molecular Weight: 591.963
• Mol File: 153172-36-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3aR,4R,6S,6aS)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-6-[2-phenylsulfanyl-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: (3aR,4R,6S,6aS)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-6-[2-phenylsulfanyl-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole(153172-36-2)
• EPA Substance Registry System: (3aR,4R,6S,6aS)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-6-[2-phenylsulfanyl-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole(153172-36-2)

Safety Data

• Hazardous Substances Data: 153172-36-2(Hazardous Substances Data)

Upstream product

• 153172-30-6 1-amino-1,4-anhydro-N-benzyl-5-O-tertbutyldimethylsilyl-1-deoxy-2,3-O-isopropylidene-D-ribitol 
• 117858-84-1 N-benzyl-1,4-dideoxy-1,4-imino-2,3-O-isopropylidene-D-ribitol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 101226-33-9 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole 
• 153172-35-1 2-(phenylthio)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole 
• 153172-33-9 (3aR,4R,6aS)-4-(((tert-butyldimethylsilyl)oxy)methyl)-2,2-dimethyl-4,6a-dihydro-3aH-[1,3]dioxolo[4,5-c]pyrrole 
• 153172-32-8 (3aR,4R,6aS)-4-(tert-Butyl-dimethyl-silanyloxymethyl)-5-chloro-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole 
• 153172-31-7 (3aR,4R,6aS)-4-({[(tert-butyl)(dimethyl)silyl]oxy}methyl)tetrahydro-2,2-dimethyl-3aH-[1,3]dioxolo[4,5-c]pyrrole 
• 882-33-7 diphenyldisulfane 

Relevant articles and documents

A new class of C-nucleoside analogues. 1-(S)-aryl-1,4-dideoxy-1,4-imino-D-ribitols, transition state analogue inhibitors of nucleoside hydrolase

The first members of new class of N-glycohydrolase transition state analogue inhibitors, 1,4-dideoxy-1,4-imino-1-(S)-phenyl-D-ribitol, 1, and 1,4-dideoxy-1,4-imino-1-(S)-(4-imidazolyl)-D-ribitol, 2, have been synthesized. The compounds represent a new typ