1112264-96-6

Basic information

• Product Name: 3-bromopropyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranoside
• Synonyms: 3-bromopropyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranoside
• CAS NO: 1112264-96-6
• Molecular Weight: 661.633
• Mol File: 1112264-96-6.mol

Chemical Properties

• CAS DataBase Reference: 3-bromopropyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromopropyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranoside(1112264-96-6)
• EPA Substance Registry System: 3-bromopropyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranoside(1112264-96-6)

Safety Data

• Hazardous Substances Data: 1112264-96-6(Hazardous Substances Data)

Upstream product

• 139974-84-8 phenyl 2,3,4,6-tetra-O-benzyl-1-thio-α-D-galactopyranoside 
• 627-18-9 1-bromo-3-propanol 
• 90358-01-3 2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl trichloroacetimidate 

Relevant articles and documents

[bmim][OTf]: a versatile room temperature glycosylation promoter

[bmim][OTf] is a versatile, ionic liquid promoter for the room temperature glycosylation of both thiophenyl and trichloroacetimidate glycoside donors; the conditions are mild, with no requirement for molecular sieves, and are compatible with a wide range

N-benzoylglycine/thiourea cooperative catalyzed stereoselective O-glycosidation: Activation of O-glycosyl trichloroacetimidate donors

A new practical utility for β-stereoselective glycosylation via activation of O-glycosyl trichloroacetimidate donors using N-benzoylglycine/thiourea cooperative catalysis has been demonstrated. This method represents the first instance where amino acid derived N-benzoylglycine is used as a catalyst for O–glycosylation under mild reaction conditions at ambient temperature. NMR spectroscopy studies suggest that thiourea cocatalyst exhibit a cooperative behaviour that has a strong effect on the reaction rate, yield, and the β-selectivity.