867151-02-8

Basic information

• Product Name: (R)-2-[1,1-Dimethyl-2-((S)-toluene-4-sulfinyl)-ethyl]-hexanoic acid tert-butyl ester
• Synonyms: (R)-2-[1,1-Dimethyl-2-((S)-toluene-4-sulfinyl)-ethyl]-hexanoic acid tert-butyl ester
• CAS NO: 867151-02-8
• Molecular Weight: 366.565
• Mol File: 867151-02-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-2-[1,1-Dimethyl-2-((S)-toluene-4-sulfinyl)-ethyl]-hexanoic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-[1,1-Dimethyl-2-((S)-toluene-4-sulfinyl)-ethyl]-hexanoic acid tert-butyl ester(867151-02-8)
• EPA Substance Registry System: (R)-2-[1,1-Dimethyl-2-((S)-toluene-4-sulfinyl)-ethyl]-hexanoic acid tert-butyl ester(867151-02-8)

Safety Data

• Hazardous Substances Data: 867151-02-8(Hazardous Substances Data)

Upstream product

• 2492-18-4 tert-butyl hexanoate 
• 867150-83-2 1-((R)-1-Chloro-2-methyl-prop-1-ene-1-sulfinyl)-4-methyl-benzene 
• 867150-95-6 tert-butyl 2-{1-[chloro(p-tolylsulfinyl)methyl]-1-methylethyl}hexanoate 

Relevant articles and documents

A novel method for asymmetric synthesis of both enantiomers of α-substituted carboxylic acid derivatives from optically active 1-chlorovinyl p-tolyl sulfoxides and lithium ester enolates with 1,4-chiral induction from the sulfur chiral center

Treatment of optically active 1-chlorovinyl p-tolyl sulfoxides, which were synthesized from symmetrical ketones and (R)-(-)-chloromethyl p-tolyl sulfoxide in three steps, with lithium enolate of carboxylic acid tert-butyl esters gave optically active addu