150424-95-6

Basic information

• Product Name: p-nitrophenyl 4-O-benzyl-2-O-<4-O-(2,4-di-O-benzyl-3,6-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-α-L-rhamnopyranosyl>-3-O-methyl-α-L-rhamnopryranoside
• CAS NO: 150424-95-6
• Molecular Weight: 934.047
• Mol File: 150424-95-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: p-nitrophenyl 4-O-benzyl-2-O-<4-O-(2,4-di-O-benzyl-3,6-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-α-L-rhamnopyranosyl>-3-O-methyl-α-L-rhamnopryranoside(CAS DataBase Reference)
• NIST Chemistry Reference: p-nitrophenyl 4-O-benzyl-2-O-<4-O-(2,4-di-O-benzyl-3,6-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-α-L-rhamnopyranosyl>-3-O-methyl-α-L-rhamnopryranoside(150424-95-6)
• EPA Substance Registry System: p-nitrophenyl 4-O-benzyl-2-O-<4-O-(2,4-di-O-benzyl-3,6-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-α-L-rhamnopyranosyl>-3-O-methyl-α-L-rhamnopryranoside(150424-95-6)

Safety Data

• Hazardous Substances Data: 150424-95-6(Hazardous Substances Data)

Upstream product

• 88043-70-3 p-nitrophenyl 2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 1226-39-7 p-nitrophenyl α-L-rhamnopyranoside 
• 150412-45-6 p-nitrophenyl 4-O-benzyl-2,3-O-isopropylidene-α-L-rhamnopyranoside 
• 150412-46-7 p-nitrophenyl 4-O-benzyl-α-L-rhamnopyranoside 
• 100-39-0 benzyl bromide 
• 150412-47-8 p-nitrophenyl 4-O-benzyl-3-O-methyl-α-L-rhamnopyranoside 
• 150412-61-6 ethyl 4-O-(2,4-di-O-benzyl-3,6-di-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-1-thio-α-L-rhamnopyranoside 

Downstream Products

• 150412-54-7 p-trifluoroacetamidophenyl 4-O-benzyl-2-O-<4-O-(2,4-di-O-benzyl-3,6-O-methyl-β-D-glucopyranosyl)-2,3-di-O-methyl-α-L-rhamnopyranosyl>-3-O-methyl-α-L-rhamnopryranoside 
• 1053616-06-0 4-{(2S,3R,4R,5S,6S)-5-Benzyloxy-3-[(2S,3R,4R,5S,6S)-5-((2S,3R,4S,5R,6R)-3,5-bis-benzyloxy-4-methoxy-6-methoxymethyl-tetrahydro-pyran-2-yloxy)-3,4-dimethoxy-6-methyl-tetrahydro-pyran-2-yloxy]-4-methoxy-6-methyl-tetrahydro-pyran-2-yloxy}-phenylamine 

Relevant articles and documents

A new approach to the chemical synthesis of the trisaccharide, and the terminal di- and mono-saccharide units of the major, serologically active glycoplipid from Mycobacterium leprae

The key intermediates for the synthesis of p-trifluoroacetamidophenyl O-(3,6-di-O-methyl-β-D-glucopyranosyl)-(1 → 4)-O-(2,3-di-O-methyl-α-L-rhamnopyranosyl)-(1 → 2)-3-O-methyl-α-L-rhamnopyranoside (15), as well as p-trifluoroacetamidophenyl O-(3,6-di-O-me