249617-06-9

Basic information

• Product Name: (2R,3S,4S)-1-Benzyl-3-(benzyloxy)-4-(tert-butyldimethylsilyloxy)-2-(4-methoxybenzyl)pyrrolidine
• Synonyms: (2R,3S,4S)-1-Benzyl-3-(benzyloxy)-4-(tert-butyldimethylsilyloxy)-2-(4-methoxybenzyl)pyrrolidine
• CAS NO: 249617-06-9
• Molecular Weight: 517.784
• Mol File: 249617-06-9.mol

Chemical Properties

• CAS DataBase Reference: (2R,3S,4S)-1-Benzyl-3-(benzyloxy)-4-(tert-butyldimethylsilyloxy)-2-(4-methoxybenzyl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S,4S)-1-Benzyl-3-(benzyloxy)-4-(tert-butyldimethylsilyloxy)-2-(4-methoxybenzyl)pyrrolidine(249617-06-9)
• EPA Substance Registry System: (2R,3S,4S)-1-Benzyl-3-(benzyloxy)-4-(tert-butyldimethylsilyloxy)-2-(4-methoxybenzyl)pyrrolidine(249617-06-9)

Safety Data

• Hazardous Substances Data: 249617-06-9(Hazardous Substances Data)

Upstream product

• 249617-04-7 Benzyl-[(1R,2S)-2-benzyloxy-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-1-(4-methoxy-benzyl)-ethyl]-amine 
• 186465-29-2 (2S,3S,4R)-4-(Benzylamino)-3-(benzyloxy)-5-(4-methoxyphenyl)pentane-1,2-diol 
• 186465-19-0 (2S,3S)-N,2-O-Dibenzyl-3,4-O-isopropylidene-L-threose imine 
• 100-46-9 benzylamine 
• 100906-42-1 2-O-benzyl-3,4-O-isopropylidene-L-threose 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 186465-39-4 (2R,3S,4S)-1-Benzyl-3-(benzyloxy)-4-hydroxy-2-(4-methoxybenzyl)pyrrolidine 

Downstream Products

• 249617-08-1 (2R,3S,4S)-1-(tert-Butoxycarbonyl)-4-(tert-butyldimethylsilyloxy)-3-hydroxy-2-(4-methoxybenzyl)pyrrolidine 
• 180081-83-8 (2R,3S,4S)-3-Acetoxy-1-(tert-butoxycarbonyl)-4-(tert-butyldimethylsilyloxy)-2-(4-methoxybenzyl)pyrrolidine 
• 22862-75-5 (2R,3S,4S)-3-(acetyloxy)-4-hydroxy-2-(4-methoxybenzyl)pyrrolidinium chloride 
• 249617-11-6 3-benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-2-(4-methoxy-benzyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

Stereoselective synthesis and biological evaluation of anisomycin and 2- substituted analogues

The naturally occurring pyrrolidine anisomycin 1, its deacetyl derivative 9k, and some previously unknown analogues were prepared from 2-O- benzyl-3,4-O-isopropylidene-L-threose 2, via the N-benzylimine 3, using highly threo-selective additions of organol