59965-19-4

Basic information

• Product Name: 1-Octanol, 3,7-dimethyl-, 4-methylbenzenesulfonate, (R)-
• CAS NO: 59965-19-4
• Molecular Formula: C17H28O3S
• Molecular Weight: 312.474
• Mol File: 59965-19-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Octanol, 3,7-dimethyl-, 4-methylbenzenesulfonate, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octanol, 3,7-dimethyl-, 4-methylbenzenesulfonate, (R)-(59965-19-4)
• EPA Substance Registry System: 1-Octanol, 3,7-dimethyl-, 4-methylbenzenesulfonate, (R)-(59965-19-4)

Safety Data

• Hazardous Substances Data: 59965-19-4(Hazardous Substances Data)

Upstream product

• 1117-61-9 (3R)-citronellol 
• 98-59-9 p-toluenesulfonyl chloride 
• 123-51-3 i-Amyl alcohol 
• 59965-17-2 (R)-1-tert-butoxy-2,6-dimethyl-heptane 
• 32531-52-5 (R)-3,7-dimethyloctanoic acid 
• 33885-93-7 (+)(R)-2.6-dimethyl-octanoic acid-⁽⁸⁾-nitrile 
• 1117-60-8 (R)-3,7-dimethyloctan-1-ol 
• 2431-75-6 isoamyl tosylate 

Downstream Products

• 6750-34-1 (3R,7R)-hexahydrofarnesol 
• 1318253-53-0 C₃₆H₆₇NO₃ 
• 1318253-54-1 3,4,5-tris((R)-3,7-dimethyloctyloxy)benzoic acid methyl ester 
• 131636-84-5 (2R,6R,10R)-6,10,14-trimethyl-5-(phenylsulfonyl)-2-(tetrahydropyranyloxy)pentadecane 
• 131636-84-5 (2S,6R,10R)-6,10,14-trimethyl-5-(phenylsulfonyl)-2-(tetrahydropyranyloxy)pentadecane 
• 131636-77-6 (2S,6R)-2,6,10-trimethyl-3-(phenylsulfonyl)-1-(tetrahydropyranyloxy)undecane 
• 131636-78-7 (2R,6R)-2,6,10-trimethylundecyl tosylate 
• 131636-82-3 (2R,6R)-2,6,10-trimethyl-1-(phenylsulfonyl)undecane 
• 131636-80-1 (2R,6R)-2,6,10-trimethyl-1-(phenylthio)undecane 

Relevant articles and documents

Total synthesis of natural α-tocopherol

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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.

Synthetic studies on (2R,4'R,8'R) α tocopherol. An approach utilizing side chain synthons of microbiological origin

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