1107017-21-9

Basic information

• Product Name: (1S,2S)-N-p-toluenesulfonyl-1,2-di(3,5-di-tert-butylphenyl)ethylenediamine
• Synonyms: (1S,2S)-N-p-toluenesulfonyl-1,2-di(3,5-di-tert-butylphenyl)ethylenediamine
• CAS NO: 1107017-21-9
• Molecular Weight: 590.914
• Mol File: 1107017-21-9.mol

Chemical Properties

• CAS DataBase Reference: (1S,2S)-N-p-toluenesulfonyl-1,2-di(3,5-di-tert-butylphenyl)ethylenediamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-N-p-toluenesulfonyl-1,2-di(3,5-di-tert-butylphenyl)ethylenediamine(1107017-21-9)
• EPA Substance Registry System: (1S,2S)-N-p-toluenesulfonyl-1,2-di(3,5-di-tert-butylphenyl)ethylenediamine(1107017-21-9)

Safety Data

• Hazardous Substances Data: 1107017-21-9(Hazardous Substances Data)

Upstream product

• 1191080-56-4 (R,R)-N,N'-((1S,2S)-1,2-bis(3,5-di-tert-butylphenyl)ethane-1,2-diyl)bis(2-methylpropane-2-sulfinamide) 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

Catalytic enantioselective synthesis of chiral phthalides by efficient reductive cyclization of 2-acylarylcarboxylates under aqueous transfer hydrogenation conditions

A new diamine ligand for asymmetric transfer hydrogenation (ATH) was discovered. The reductive cyclization of 2-acylarylcarboxylates was found to proceed highly stereoselective by the new Ru complex-catalyzed ATH and subsequent In situ lactonization under aqueous conditions. It enables efficient access to a wide variety of 3-substituted phthalides In enantiomerically pure form.