175025-14-6

Basic information

• Product Name: (S,S)-2,6-bis((α-p-toluenesulfonyloxy)ethyl)pyridine
• Synonyms: (S,S)-2,6-bis((α-p-toluenesulfonyloxy)ethyl)pyridine
• CAS NO: 175025-14-6
• Molecular Weight: 475.587
• Mol File: 175025-14-6.mol

Chemical Properties

• CAS DataBase Reference: (S,S)-2,6-bis((α-p-toluenesulfonyloxy)ethyl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: (S,S)-2,6-bis((α-p-toluenesulfonyloxy)ethyl)pyridine(175025-14-6)
• EPA Substance Registry System: (S,S)-2,6-bis((α-p-toluenesulfonyloxy)ethyl)pyridine(175025-14-6)

Safety Data

• Hazardous Substances Data: 175025-14-6(Hazardous Substances Data)

Upstream product

• 143329-85-5 (R,R)-α,α'-dimethyl-2,6-pyridinedimethanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 1129-30-2 2,6-Diacetylpyridine 

Relevant articles and documents

Synthesis of (1R, 1R')-2,6-bis[1-(diphenylphosphino)ethyl]pyridine and its application in asymmetric transfer hydrogenation

A C2 symmetric tridentate ligand, (1R, 1R') 2,6-Bis[1-(diphenylphosphino)ethyl]pyridine, has been synthesized in enantiomerically pure form. A practical method to synthesize a variety of chiral pyridyl diols is reported. Asymmetric transfer hydrogenation is achieved using the tridentate ligand.

Stereocomplexity and stereoselective synthesis of triamine molecules bearing four chiral carbon centers: Stereodifferentiated preparation of all 10 stereoisomers of 2,6-bis[1-(1-phenylethylamino)ethyl]pyridines

Compounds (S,S)-2,6-bis(1-hydroxyethyl)pyridine, (R,R)-2,6-bis(1- acetoxyethyl)pyridine, and (1R,1′S)-2-(1-acetoxyethyl)-6-(1′- hydroxyethyl)pyridine were obtained by lipase-catalyzed kinetic acetylation of 2,6-bis(1-hydroxyethyl)pyridine as enantiomerica