79507-60-1

Basic information

• Product Name: 3,4-di-O-acetyl-1,6-bis-O-(methylsulfonyl)hex-2-ulofuranosyl 3,4-di-O-acetyl-2,6-bis-O-(methylsulfonyl)hexopyranoside
• CAS NO: 79507-60-1
• Molecular Formula: C₂₄H₃₈O₂₃S₄
• Molecular Weight: 822.8047
• Mol File: 79507-60-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 943.8°C at 760 mmHg
• Flash Point: 524.6°C
• Density: 1.58g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.545
• CAS DataBase Reference: 3,4-di-O-acetyl-1,6-bis-O-(methylsulfonyl)hex-2-ulofuranosyl 3,4-di-O-acetyl-2,6-bis-O-(methylsulfonyl)hexopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-di-O-acetyl-1,6-bis-O-(methylsulfonyl)hex-2-ulofuranosyl 3,4-di-O-acetyl-2,6-bis-O-(methylsulfonyl)hexopyranoside(79507-60-1)
• EPA Substance Registry System: 3,4-di-O-acetyl-1,6-bis-O-(methylsulfonyl)hex-2-ulofuranosyl 3,4-di-O-acetyl-2,6-bis-O-(methylsulfonyl)hexopyranoside(79507-60-1)

Safety Data

• Hazardous Substances Data: 79507-60-1(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 124-63-0 methanesulfonyl chloride 
• 57-50-1 Sucrose 

Relevant articles and documents

Transformation of Sucrose: An Alternative Route for Amination

Mesylation of sucrose with 1 and 2 moles of mesylchloride (methane sulfonyl chloride) separately followed by acetylation in pyridine formed mono-, di-, tri- and tetra-O-mesyl sucrose-acetates respectively.Mono and dimesyl sucrose-acetates are converted into their amino derivatives via iodo and azido compounds in appreciable yields.