133646-16-9

Basic information

• Product Name: 4-chloro-N-(2,3,4,6-tetra-O-pivaloyl-α-D-galactopyranosyl)-D-phenylglycinotrile
• CAS NO: 133646-16-9
• Molecular Weight: 665.224
• Mol File: 133646-16-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-chloro-N-(2,3,4,6-tetra-O-pivaloyl-α-D-galactopyranosyl)-D-phenylglycinotrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-N-(2,3,4,6-tetra-O-pivaloyl-α-D-galactopyranosyl)-D-phenylglycinotrile(133646-16-9)
• EPA Substance Registry System: 4-chloro-N-(2,3,4,6-tetra-O-pivaloyl-α-D-galactopyranosyl)-D-phenylglycinotrile(133646-16-9)

Safety Data

• Hazardous Substances Data: 133646-16-9(Hazardous Substances Data)

Upstream product

• 108342-86-5 2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl azide 
• 108342-85-4 1,2,3,4,6-penta-O-pivaloyl-β-D-galactopyranose 
• 143-33-9 sodium cyanide 
• 104-88-1 4-chlorobenzaldehyde 
• 108342-87-6 tetra-O-pivaloyl-β-D-galactopyranosylamine 

Relevant articles and documents

Carbohydrates as Chiral Templates: Stereoselective Strecker Synthesis of D-α-Amino Nitriles and Acids Using O-Pivaloylated D-Galactosylamine as the Auxiliary

The asymmetric synthesis of N-galactosyl D-α-amino nitriles is accomplished by application of 2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosylamine (4) as the stereodifferentiating template in Strecker reactions.Aldimines 6 derived from 4 and aromatic or ali