133644-99-2

Basic information

• Product Name: (2S,3S)-dihydroxy-1,4-diphenylbutane
• Synonyms: (2S,3S)-dihydroxy-1,4-diphenylbutane
• CAS NO: 133644-99-2
• Molecular Weight: 242.318
• Mol File: 133644-99-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S,3S)-dihydroxy-1,4-diphenylbutane(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S)-dihydroxy-1,4-diphenylbutane(133644-99-2)
• EPA Substance Registry System: (2S,3S)-dihydroxy-1,4-diphenylbutane(133644-99-2)

Safety Data

• Hazardous Substances Data: 133644-99-2(Hazardous Substances Data)

Upstream product

• 298-18-0 (S,S)-diepoxybutane 
• 100-58-3 phenylmagnesium bromide 
• 13657-49-3 1,4-diphenylbut-2-ene 

Downstream Products

• 219616-86-1 (4S,5S)-4,5-bis(phenylmethyl)-2-phenylselenomethyl-1,3-dioxolan 
• 219650-24-5 (4S,5S)-2-bromomethyl-4,5-bis(phenylmethyl)-1,3-dioxolan 

Relevant articles and documents

The attempted stereoselective synthesis of chiral 2,2′-biindoline

The attempted first stereoselective synthesis of 2,2′-biindoline using a metathesis-Sharpless asymmetric dihydroxylation strategy results in the synthesis of the heterocycle in poor to modest stereoselectivity. Attempts to improve the ee by varying the he

Synthesis of chiral nonracemic diols via nucleophilic opening of (S,S)-1,2,3,4-diepoxybutane

(S,S)-1,2,3,4-diepoxybutane was synthesized from (R,R)-dimethyl tartrate. Nucleophilic opening of this diepoxybutane gave a convenient method for generating a variety of chiral nonracemic diols.