146399-93-1

Basic information

• Product Name: butyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside
• Synonyms: butyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside
• CAS NO: 146399-93-1
• Molecular Weight: 652.698
• Mol File: 146399-93-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: butyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: butyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside(146399-93-1)
• EPA Substance Registry System: butyl 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranoside(146399-93-1)

Safety Data

• Hazardous Substances Data: 146399-93-1(Hazardous Substances Data)

Upstream product

• 14218-11-2 2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide 
• 71-36-3 butan-1-ol 
• 149707-75-5 2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl trichloroacetimidate 
• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 
• 98-88-4 benzoyl chloride 
• 5391-18-4 n-butyl β-D-glucopyranoside 
• 6697-88-7 2,3,4,6-tetra-O-acetyl-1-n-butyl-β-D-glucopyranoside 
• 2592-58-7 1,2,3,4,6-penta-O-benzoyl-D-glucopyranoside 
• 66530-18-5 2,3,4,6-tetra-O-benzoyl-α-D-glucopyranose 

Downstream Products

• 1246854-71-6 butyl 2,3,4,6-tetra-O-benzoyl-α-D-glucopyranoside 
• 146453-36-3 butyl α-D-mannopyranoside 

Relevant articles and documents

Large-scale synthesis of D-mannose 6-phosphate and other hexose 6-phosphates

The syntheses of D-mannose 6-phosaphate (4), several D-mannopyranoside 6-phosphates, and methyl α-D-glucopyranoside 6-phosphate are described.Phophorylation of methyl 2,3,4-tri-O-(trimethylsilyl)-α-D-mannopyranoside (2) with phosphorus oxychloride followe

Influence of acyl groups on glucopyranoside reactivity in Lewis acid promoted anomerisation

Lewis acid promoted anomerisation has potential in O- or S-glycoside synthesis. Herein, the anomerisation kinetics of thirty-one β-D-glucopyranosides was determined to determine how particular acyl protecting groups and their location influence reactivity towards a Lewis acid promoted reaction. The replacement of acetyl groups with benzoyl groups led to reduced reactivity when located at O-3, O-4 and O-6. However a reactivity increase was observed when the acetyl group was replaced by a benzoyl group at O-2. The 2,3,4,6-tetra-O-(4-methoxy)benzoate had an ～2-fold increase in rate when compared to the tetrabenzoate.

ANTI-ADHESIVE COMPOUNDS TO PREVENT AND TREAT BACTERIAL INFECTIONS

The present invention provides compounds and compositions capable of inhibiting the attachment of Gram-negative bacteria on a host epithelium. Accordingly, said compounds and compositions can for example be used for the manufacture of a medicament to trea