1277151-49-1

Basic information

• Product Name: benzyl 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl diisopropylphosphoramidite
• Synonyms: benzyl 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl diisopropylphosphoramidite
• CAS NO: 1277151-49-1
• Molecular Weight: 780.3
• Mol File: 1277151-49-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl diisopropylphosphoramidite(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl diisopropylphosphoramidite(1277151-49-1)
• EPA Substance Registry System: benzyl 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl diisopropylphosphoramidite(1277151-49-1)

Safety Data

• Hazardous Substances Data: 1277151-49-1(Hazardous Substances Data)

Upstream product

• 89807-86-3 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-decan-1-ol 
• 108549-21-9 benzyl-N,N,N',N'-tetraisopropylphosphorodiamidite 

Downstream Products

• 1277151-61-7 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-(benzyl 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl phosphate)-β-D-galactopyranoside 
• 1277151-59-3 2-(trimethylsilyl)ethyl 2,4-di-O-benzyl-6-(benzyl 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl phosphate)-3-O-p-methoxybenzyl-β-D-galactopyranoside 
• 1277151-55-9 6-(benzyl ammonium phosphate)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 1277151-54-8 6-(benzyl 2-bromo-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl phosphate)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 

Relevant articles and documents

A fluorous phosphate protecting group with applications to carbohydrate synthesis

The first fluorous protecting group for phosphate is reported. This group can be used as a facile tag for purification and be removed under mild reducing conditions using zinc and ammonium formate. Synthesis of a disaccharide from Leishmania using this fluorous protecting group demonstrated the group's stability to the acidic conditions necessary for glycosylation as well as its orthogonality to several other common protecting groups.