116013-69-5

Basic information

• Product Name: 1-Octanol, 2-methyl-, (S)-
• CAS NO: 116013-69-5
• Molecular Formula: C9H20O
• Molecular Weight: 144.257
• Mol File: 116013-69-5.mol

Chemical Properties

• CAS DataBase Reference: 1-Octanol, 2-methyl-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octanol, 2-methyl-, (S)-(116013-69-5)
• EPA Substance Registry System: 1-Octanol, 2-methyl-, (S)-(116013-69-5)

Safety Data

• Hazardous Substances Data: 116013-69-5(Hazardous Substances Data)

Upstream product

• 59983-39-0 (S)-1-amino-2-(methoxymethyl)pyrrolidine 
• 152899-14-4 <3(2'S),4S>-3-(2-Methyl-1-oxooctyl)-4-(phenylmethyl)-2-oxazolidinone 

Downstream Products

• 7786-29-0 (S)-α-methyloctanal 
• 117555-29-0 (S)-2-Methyl-1-octanol tosylate 
• 569353-65-7 (S)-(+)-4-[1-(2-methyl)octyloxy]phenyl benzoate 
• 569353-66-8 (S)-(+)-4-[1-(2-methyl)octyloxy]phenol 
• 254435-71-7 (S)-3-methyl-1-(phenylsulfonyl)nonane 
• 328547-79-1 (5R,7RS,9S)-5,9-dimethyl-7-(phenylsulfonyl)pentadecane 
• 328547-76-8 (5S,7RS,9S)-5,9-dimethyl-7-(phenylsulfonyl)pentadecane 
• 254435-73-9 (7R,9RS,11S)-7,11-dimethyl-9-phenylsulfonylheptadecane 
• 254435-74-0 (7S,9RS,11S)-7,11-dimethyl-9-phenylsulfonylheptadecane 
• 153077-12-4 (2E,4E)-(S)-4,6-Dimethyl-dodeca-2,4-dienoic acid [(S)-1-formyl-2-(4-hydroxy-phenyl)-ethyl]-amide 
• 153077-11-3 Ethyl (2S,2'E,4'E,6'S)-2-(4,6-dimethyldodeca-2,4-dienoylamido)-3-(4-hydroxyphenyl)propanoate 
• 117184-53-9 Epiaranorosin 
• 117184-53-9 6'-epi-Aranorosin 
• 117184-53-9 6'-epiaranorosin 

Relevant articles and documents

An efficient strategy for the synthesis of chiral liquid crystals using Evans' methodology

The synthesis of liquid crystal compound 2 was achieved using Evans' methodology. The strategy was based on three key synthetic reactions: alkylation of chiral amide enolates, Mitsunobu and, finally, esterification. The final compound presents a stable smectic A phase.

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.