1289154-21-7

Basic information

• Product Name: (-)-[(S)-N-(p-tolylsulfonyl)-2-pyrrolidinyl]propyl-2,3,4-tri-O-benzyl-β-L-fucopyranoside
• Synonyms: (-)-[(S)-N-(p-tolylsulfonyl)-2-pyrrolidinyl]propyl-2,3,4-tri-O-benzyl-β-L-fucopyranoside
• CAS NO: 1289154-21-7
• Molecular Weight: 699.909
• Mol File: 1289154-21-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (-)-[(S)-N-(p-tolylsulfonyl)-2-pyrrolidinyl]propyl-2,3,4-tri-O-benzyl-β-L-fucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-[(S)-N-(p-tolylsulfonyl)-2-pyrrolidinyl]propyl-2,3,4-tri-O-benzyl-β-L-fucopyranoside(1289154-21-7)
• EPA Substance Registry System: (-)-[(S)-N-(p-tolylsulfonyl)-2-pyrrolidinyl]propyl-2,3,4-tri-O-benzyl-β-L-fucopyranoside(1289154-21-7)

Safety Data

• Hazardous Substances Data: 1289154-21-7(Hazardous Substances Data)

Upstream product

• 242805-31-8 allyl 2,3,4-tri-O-benzyl-L-fucopyranoside 
• 242805-30-7 O-allyl-L-fucopyranose 
• 147-85-3 L-proline 
• 23356-96-9 (S)-1-Pyrrolidin-2-yl-methanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 52682-03-8 (S)(-)-N,O-bis(p-toluenesulphonyl)-2-hydroxymethyl pyrrolidine 
• 162118-38-9 (3S,4R,5R,6S)-3,4,5-tris(benzyloxy)-6-methyltetrahydro-2H-pyran-2-ol 
• 100-39-0 benzyl bromide 
• 73-34-7 6-deoxy-L-galactose 
• 1289154-19-3 (-)-[(S)-N-(p-tolylsulfonyl)-2-pyrrolidinyl]propan-1-ol 
• 120703-59-5 O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)trichloroacetimidate 
• 1289154-18-2 (-)methyl [(S)-N-(p-tolylsulfonyl)-2-pyrrolidinyl]propionate 
• 1289154-17-1 (-)dimethyl [(S)-N-(p-tolylsulfonyl)-2-pyrrolidinyl]methyl malonate 

Relevant articles and documents

Synthesis of new [(2S)-N-(p-Tolylsulfonyl)-2-Pyrrolidinyl]Propyl 2,3,4-Tri-O-Acetyl- and 2,3,4-Tri-O-Benzyl-β-L-Fucopyranosides

Synthesis of two new glycoheterocyclic compounds, [(2S)-N-(p-tolylsulfonyl) -2-pyrrolidinyl]propyl 2,3,4-tri-O-acetyl- and 2,3,4-tri-O-benzyl-β-L- fucopyranosides la and lb, starting from δ-amino alcohol (-)-[(2S)-N-(ptolylsulfonyl)-2-pyrrolidinyl]propan-l-ol 2 and O-α-L-fucosyltrichloroacetimidates 3a or 3b as glycosyl donor is described. Hitherto δ-aminoalcohol 2 was synthesized from L-proline without any racemization during its preparation.