117555-29-0

Basic information

• Product Name: 1-Octanol, 2-methyl-, 4-methylbenzenesulfonate, (S)-
• CAS NO: 117555-29-0
• Molecular Formula: C16H26O3S
• Molecular Weight: 298.447
• Mol File: 117555-29-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Octanol, 2-methyl-, 4-methylbenzenesulfonate, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octanol, 2-methyl-, 4-methylbenzenesulfonate, (S)-(117555-29-0)
• EPA Substance Registry System: 1-Octanol, 2-methyl-, 4-methylbenzenesulfonate, (S)-(117555-29-0)

Safety Data

• Hazardous Substances Data: 117555-29-0(Hazardous Substances Data)

Upstream product

• 116013-69-5 (2S)-2-methyloctan-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 72203-94-2 N-[(S)-2-methoxymethylpyrrolidin-1-yl]propan-1-imine 
• 59983-39-0 (S)-1-amino-2-(methoxymethyl)pyrrolidine 
• 446276-90-0 ((S)-2-Methoxymethyl-pyrrolidin-1-yl)-[(S)-2-methyl-oct-(E)-ylidene]-amine 
• 693-25-4 n-pentylmagnesium bromide 
• 177088-50-5 (S)-2-methyl-1-octanol tetrahydropyranyl ether 
• 818-81-5 2-methyloctan-1-ol 
• 3004-93-1 2-methyloctanoic acid 
• 2177-86-8 methyl 2-methyloctanoate 
• 4360-86-5 2-hexyl-2-methylmalonic acid 
• 64770-20-3 2-hexyl-2-methylmalonic acid diethyl ester 

Downstream Products

• 254435-71-7 (S)-3-methyl-1-(phenylsulfonyl)nonane 
• 254435-73-9 (7R,9RS,11S)-7,11-dimethyl-9-phenylsulfonylheptadecane 
• 254435-74-0 (7S,9RS,11S)-7,11-dimethyl-9-phenylsulfonylheptadecane 
• 17001-26-2 (10RS)-10-methylhexadecanoic acid 

Relevant articles and documents

Asymmetric synthesis of all stereoisomers of 7,11-dimethylheptadecane and 7-methylheptadecane, the female pheromone components of the spring hemlock looper and the pitch pine looper

The asymmetric synthesis of the stereoisomers of 7,11-dimethylheptadecane (1) and 7-methylheptadecane (2) via α-alkylation employing the SAMP/RAMP hydrazone method with high asymmetric induction and good overall yields is described. A mixture of (7S,11R)-1 and (S)-2 is the female-produced sex pheromone of the spring hemlock looper moth (Lambdina athasaria) and the pitch pine looper moth (Lambdina pellucidaria). They are both forest pests in northeastern North America.

Pheromone synthesis, CLXXIV: Synthesis of (5R,11S)-5,11-Dimethylheptadecane and (S)-2,5-Dimethylheptadecane, the major and the minor components of the sex pheromone of the geometrid moth, Lambdina fiscellaria lugubrosa

(5R,11S)-5,11-Dimethylheptadecane (1), the major component of the female-produced sex pheromone of the western hemlock looper (Lambdina fiscellaria lugubrosa), was synthesized by starting from the enantiomers of methyl 3-hydroxy-2-methylpropanoate (3). (S)-2,5-Dimethylheptadecane (2), the minor and synergistic component of the pheromone, was also synthesized by starting from (S)-citronellol (4). VCH Verlagsgesellschaft mbH, 1996.

Synthesis of methyl branched fatty acid

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