1021348-20-8

Basic information

• Product Name: (1S,2S)-1,2-bis(4-bromophenyl)-2-(phenylselanyl)ethanol
• CAS NO: 1021348-20-8
• Molecular Weight: 511.114
• Mol File: 1021348-20-8.mol

Chemical Properties

• CAS DataBase Reference: (1S,2S)-1,2-bis(4-bromophenyl)-2-(phenylselanyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-1,2-bis(4-bromophenyl)-2-(phenylselanyl)ethanol(1021348-20-8)
• EPA Substance Registry System: (1S,2S)-1,2-bis(4-bromophenyl)-2-(phenylselanyl)ethanol(1021348-20-8)

Safety Data

• Hazardous Substances Data: 1021348-20-8(Hazardous Substances Data)

Upstream product

• 645-96-5 Benzeneselenol 
• 72726-46-6 tert-butyl(dimethyl)(phenylseleno)silane 

Relevant articles and documents

Synthesis of enantiomerically enriched β-hydroxy selenides by catalytic asymmetric ring opening of meso-epoxides with (phenylseleno)silanes

The first example of the enantioselective ring opening of meso-epoxides by (phenylseleno)silanes using salen(Cr)complexes as catalyst is described. This desymmetrization reaction constitutes a simple and convenient approach to synthetically versatile optically active β-hydroxy selenides.

Scandium-bipyridine-catalyzed, enantioselective selenol addition to aromatic meso-epoxides

A chiral scandium-bipyridine complex catalyzes the highly enantioselective addition of phenylselenol to aromatic meso-epoxides and furnishes 1,2-seleno alcohols in good yields and up to 94% ee. In addition, a sequential, one-pot epoxide opening-reduction