186641-91-8

Upstream product

• 101382-88-1 (2S,6R)-7-tert-butyldiphenylsilyloxy-2,6-dimethyl-1-heptanol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 186641-94-1 ((2R,6S)-7-Bromo-2,6-dimethyl-heptyloxy)-tert-butyl-diphenyl-silane 
• 186641-97-4 [(2R,6S)-8-Benzenesulfonyl-2,6-dimethyl-8-(2,6,6-trimethyl-cyclohex-1-enyl)-octyloxy]-tert-butyl-diphenyl-silane 
• 186642-00-2 tert-Butyl-[(2R,6S)-2,6-dimethyl-8-(2,6,6-trimethyl-cyclohex-1-enyl)-octyloxy]-diphenyl-silane 
• 186642-07-9 (E)-(5R,9S)-5,9-Dimethyl-11-(2,6,6-trimethyl-cyclohex-1-enyl)-undec-2-enoic acid ethyl ester 
• 186642-05-7 (3S,7R)-1-(8-cyano-3,7-dimethyloctyl)-2,6,6-trimethyl-1-cyclohexene 
• 186642-06-8 (3S,7R)-1-(3,7-dimethyl-8-formyl-octyl)-2,6,6-trimethyl-1-cyclohexene 
• 186642-03-5 (3S,7R)-1-(8-bromo-3,7-dimethyloctyl)-2,6,6-trimethyl-1-cyclohexene 

Relevant academic research and scientific papers

Synthesis of optically active diastereomers of a nonproteic neurotrophic mimetic

The four diastereomers 3, elongated analogues of perhydroretinol, are synthesized starting from both optically pure 3-bromo-2-methyl-1-propanol enantiomers. All exhibit neurotrophic activity on cultured neuronal cells derived from fetal rat cerebral hemispheres.