141882-88-4

Basic information

• Product Name: 2-Ethylsulfanylmethyl-benzoic acid (2S,3R,4S,5R,6R)-3,4,5-tris-(2,2-dimethyl-propionyloxy)-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-2-yl ester
• CAS NO: 141882-88-4
• Molecular Weight: 694.884
• Mol File: 141882-88-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Ethylsulfanylmethyl-benzoic acid (2S,3R,4S,5R,6R)-3,4,5-tris-(2,2-dimethyl-propionyloxy)-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-2-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Ethylsulfanylmethyl-benzoic acid (2S,3R,4S,5R,6R)-3,4,5-tris-(2,2-dimethyl-propionyloxy)-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-2-yl ester(141882-88-4)
• EPA Substance Registry System: 2-Ethylsulfanylmethyl-benzoic acid (2S,3R,4S,5R,6R)-3,4,5-tris-(2,2-dimethyl-propionyloxy)-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-2-yl ester(141882-88-4)

Safety Data

• Hazardous Substances Data: 141882-88-4(Hazardous Substances Data)

Upstream product

• 7115-89-1 2-(bromomethyl)benzoic acid 
• 81058-27-7 2,3,4,6-tetra-O-pivaloyl-α-D-glucopyranosyl bromide 
• 79313-52-3 2-Ethylsulfanylmethyl-benzoic acid 

Relevant articles and documents

Stereoselective synthesis of β-1-O-acyl derivatives of carbohydrates: An application of the cesium effect

The stereoselective formation of anomerically pure 1-O-acyl derivatives of protected carbohydrates is achieved by reaction of the α-glycosyl halogenoses with cesium caboxylates.