946416-33-7

Basic information

• Product Name: methyl 2-bromo-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside
• Synonyms: methyl 2-bromo-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside
• CAS NO: 946416-33-7
• Molecular Weight: 645.59
• Mol File: 946416-33-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 2-bromo-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-bromo-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside(946416-33-7)
• EPA Substance Registry System: methyl 2-bromo-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside(946416-33-7)

Safety Data

• Hazardous Substances Data: 946416-33-7(Hazardous Substances Data)

Upstream product

• 4132-26-7 2,3,4,6-tetra-O-benzyl 1,5-anhydro-D-arabino-hex-1-enitol 
• 946416-32-6 1,5-anhydro-2,3,4,6-tetra-O-benzyl-1,2-C-(dibromomethylene)-α-D-glycero-D-galacto-hexitol 
• 124-41-4 sodium methylate 

Downstream Products

• 946416-34-8 methyl 2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1383956-18-0 methyl 2-deoxy-2-C-phenyl-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1383956-17-9 methyl 2-deoxy-2-C-(2-phenylallyl)-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1383956-21-5 methyl 2-deoxy-2-C-(2-phenylethynyl)-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1383956-19-1 methyl 2-deoxy-2-C-(p-methoxyphenyl)-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1383956-20-4 methyl 2-deoxy-2-C-(m-tolyl)-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1383956-22-6 methyl 2-deoxy-2-C-(octyn-1-yl)-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 946416-36-0 methyl 4,5,7-tri-O-benzyl-α-D-glycero-D-talo-septanoside 
• 946416-35-9 methyl 4,5,7-tri-O-benzyl-α-D-manno-sept-3-uloside 

Relevant articles and documents

Branching out at C-2 of septanosides. Synthesis of 2-deoxy-2-C-alkyl/aryl septanosides from a bromo-oxepine

This paper deals with the synthesis of 2-deoxy-2-C-alkyl/aryl septanosides. A range of such septanoside derivatives was synthesized by using a common bromo-oxepine intermediate, involving C-C bond forming organometallic reactions. Unsaturated, sevenmember