110500-32-8

Basic information

• Product Name: 1-Octanol, 2-fluoro-, (2S)-
• CAS NO: 110500-32-8
• Molecular Formula: C8H17FO
• Molecular Weight: 148.221
• Mol File: 110500-32-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Octanol, 2-fluoro-, (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Octanol, 2-fluoro-, (2S)-(110500-32-8)
• EPA Substance Registry System: 1-Octanol, 2-fluoro-, (2S)-(110500-32-8)

Safety Data

• Hazardous Substances Data: 110500-32-8(Hazardous Substances Data)

Upstream product

• 77495-66-0 (R)-1,2-epoxyoctane 

Downstream Products

• 126315-41-1 2,3-Difluoro-4-(2-fluorooctyloxy)benzoic acid 
• 119259-50-6 (S)-2-fluoro-1-p-toluenesulfonyloxyoctane 
• 116528-89-3 4'-Octyloxy-biphenyl-4-carboxylic acid 4-(2-fluoro-octyloxycarbonyl)-phenyl ester 
• 116528-97-3 4'-(4-Octyloxy-benzoyloxy)-biphenyl-4-carboxylic acid 2-fluoro-octyl ester 
• 116528-92-8 4-Octyloxy-benzoic acid 4'-(2-fluoro-octyloxy)-biphenyl-4-yl ester 
• 113701-86-3 (-)-p-(2-fluorooctyl)phenyl p'-decyloxybenzoate 
• 113701-96-5 (+)-2-fluorooctyl p-hydroxybenzoate 
• 114069-14-6 (+)-p-2-fluorooctyloxyphenol 
• 118406-60-3 (S)-2-Fluoro-octanoic acid 4-(5-dodecyl-pyrimidin-2-yl)-phenyl ester 
• 118406-54-5 (+)-5-Decyl-2-pyrimidine 
• 118406-59-0 (S)-2-Fluoro-octanoic acid 4-(5-nonyl-pyrimidin-2-yl)-phenyl ester 
• 118406-58-9 (S)-2-Fluoro-octanoic acid 4-(5-octyl-pyrimidin-2-yl)-phenyl ester 
• 129894-68-4 (+)-5-Dodecyl-2-pyrimidine 
• 129832-74-2 5-Decyl-2-[4-((S)-2-fluoro-octyloxy)-phenyl]-pyrimidine 

Relevant articles and documents

Stereo- and regiocontrolled synthesis of fluorohydrins from optically active epoxides

The hydrofluorination of optically active terminal epoxides, which were produced by a microbial reaction, with HF-amine reagents weer studied. 1,2-Epoxyoctane and glycidyl hexyl ether gave the corresponding 2-fluoro-1-alkanol derivatives with inversion of the asymmetric center with high stereospecificity, while in the hydrofluorination of pentafluorostyrene oxide and 2-methyl-1,2-epoxyhexane, partial racemization occurred. The basicity of the amine used, the HF/amine ratio in the HF-amine reagent, and the substituent on the epoxide affected the stereospecificity and regioselectivity of the hydrofluorination of the epoxides.