1379776-89-2

Basic information

• Product Name: 4-nitrophenyl 2-O-phenoxythiocarbonyl-α-D-glucopyranoside
• Synonyms: 4-nitrophenyl 2-O-phenoxythiocarbonyl-α-D-glucopyranoside
• CAS NO: 1379776-89-2
• Molecular Weight: 437.427
• Mol File: 1379776-89-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-nitrophenyl 2-O-phenoxythiocarbonyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-nitrophenyl 2-O-phenoxythiocarbonyl-α-D-glucopyranoside(1379776-89-2)
• EPA Substance Registry System: 4-nitrophenyl 2-O-phenoxythiocarbonyl-α-D-glucopyranoside(1379776-89-2)

Safety Data

• Hazardous Substances Data: 1379776-89-2(Hazardous Substances Data)

Upstream product

• 1005-56-7 phenylcarbonochloridothioate 
• 3767-28-0 4-nitrophenyl-α-D-glucopyranoside 
• 2492-87-7 4-nitrophenyl-β-D-glucoside 

Relevant articles and documents

Α- [...] compd. manufacturing method

PROBLEM TO BE SOLVED: To provide a method for producing an α-pyranoside thiocarbonyl ester compound, in which the hydroxyl group at position 2 is selectively protected. SOLUTION: An α-pyranoside compound represented by general formula (I) or general

Organotin-catalyzed highly regioselective thiocarbonylation of nonprotected carbohydrates and synthesis of deoxy carbohydrates in a minimum number of steps

Nonprotected carbohydrates: The catalytic regioselective thiocarbonylation of carbohydrates by using organotin dichloride under mild conditions was demonstrated. The reaction afforded various deoxy saccharides in high yields and excellent regioselectivity in a minimum number of steps. The regioselectivity of the thiocarbonylation is attributed to the intrinsic character of the carbohydrates based on the stereorelationship of their hydroxy groups (see scheme). Copyright