131636-79-8

Upstream product

• 79434-99-4 (2S,6S)-2,6,10-trimethyl-1-undecanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 
• 131722-96-8 (S)-4,8-dimethyl-7-nonanoic acid 
• 133732-61-3 (S)-3,7-dimethyl-1-phenylthiooctane 
• 131723-00-7 (2S,6S)-2,6,10-trimethyl-1-(tetrahydropyranyloxy)undecane 
• 131636-77-6 (2R,6S)-2,6,10-trimethyl-3-(phenylsulfonyl)-1-(tetrahydropyranyloxy)undecane 
• 68680-98-8 S-(-)-dihydrocitronellol 
• 133732-65-7 (2S,6S)-1-methoxymethoxy-2,6,10-trimethylundecane 
• 112571-88-7 (S)-1-iodo-3,7-dimethyloctane 
• 133732-64-6 (2S,4RS,6S)-1-methoxymethoxy-2,6,10-trimethyl-4-phenylsulphonylundecane 
• 133732-62-4 (S)-3,7-dimethyl-1-phenylsulphonyloctane 

Downstream Products

• 131636-84-5 (2R,6S,10S)-6,10,14-trimethyl-5-(phenylsulfonyl)-2-(tetrahydropyranyloxy)pentadecane 
• 131636-84-5 (2S,6S,10S)-6,10,14-trimethyl-5-(phenylsulfonyl)-2-(tetrahydropyranyloxy)pentadecane 
• 131636-83-4 (2S,6S)-2,6,10-trimethyl-1-(phenylsulfonyl)undecane 
• 69729-17-5 (2RS,6S,10S)-6,10,14-trimethylpentadecan-2-ol 
• 131636-81-2 (2S,6S)-2,6,10-trimethyl-1-(phenylthio)undecane 

Relevant academic research and scientific papers

Synthesis of Chiral Alcohol and Ester Pheromones through Enzyme-Catalysed Hydrolysis using Pseudomonas fluorescens Lipase: Preparation of (2R,6S,10S)-6,10,14-Trimethylpentadecan-2-ol and the Propionate of (2R,8R)-8-Methyldecan-2-ol

(2R,6S,10S)-6,10,14-Trimethylpentadecan-2-ol , one of the stereoisomers of the sex pheromone of Corcyra cephalonica Stainton, was synthesized in highly optically pure form by the hydrolysis of the 2,2,2-trichloroethyl carbonate of (2RS,6S,

Pheromone Synthesis, CXXVI. Synthesis and Biological Activity of Four Stereoisomers of 6,10,14-Trimethyl-2-pentadecanol, the Female-Produced Sex Pheromone of Rice Moth (Corcyra cephalonica)

The synthesis of four stereoisomers of the female-produced sex pheromone of the rice moth (Corcyra cephalonica) was achieved by starting from (R)-2a, (R)- or (S)-3a, and (R)- or (S)-4 and using alkylation of alkyl phenyl sulfones as the coupling reaction.Behavioral bioassy of each isomer revealed (2R,6R,10R)-1a to be eight times more active than a diastereomeric mixture of equal amounts of the eight possible stereoisomers, indicating that (2R,6R,10R)-1a is probably the natural pheromone or at least themajor component of the female blend.Electrophysiological bioassy also confirmed the high activity of (2R,6R,10R)-1a.