1578-57-0

Upstream product

• 17841-31-5 2-fluoro hexane-1-oate d'ethyle 
• 70387-20-1 1,1-bis-ethylsulfanyl-2-fluoro-hex-1-ene 
• 108200-51-7 1-Methoxy-1-(phenylthio)-2-fluoro-1-hexene 
• 615-96-3 Ethyl 2-bromohexanoate 
• 108200-51-7 monofluoroketene hemithioacetal 
• 1578-77-4 diethyl 2-butyl-2-fluoromalonate 

Downstream Products

• 26450-58-8 1,1-dimethoxy-pentane 
• 108545-24-0 (S)-N-((R)-α-hydroxymethylbenzyl)-2-fluoro-2-methylhexanamide 
• 108545-23-9 (R)-N-((R)-α-hydroxymethylbenzyl)-2-fluoro-2-methylhexanamide 
• 936111-34-1 C₃₆H₄₇FO₄SSi 
• 936111-26-1 C₃₅H₄₅FO₅SSi 

Relevant academic research and scientific papers

Electrolytic Reactions of Fluoro Organic Compounds. 7. Anodic Methoxylation and Acetoxylation of 2,2,2-Trifluoroethyl Sulfides. Preparation of Highly Useful Trifluoromethylated Building Blocks

Anodic methoxylation and acetoxylation of 2,2,2-trifluoroethyl sulfides and the corresponding nonfluorinated sulfides were comparatively studied.It was found that a trifluoromethyl group remarkably promoted anodic substitution and methoxy and acetoxy groups were introduced adjacent to the trifluoromethyl group of the sulfides.Longer perfluoroalkyl groups also promoted these anodic substitutions.These products were shown to be highly useful building blocks fro the synthesis of fluoro organic compounds.

ELECTROLYTIC TRANSFORMATION OF FUNCTIONAL GROUPS OF FLUOROORGANIC COMPOUNDS. I. ANODIC METHOXYLATION AND ACETOXYLATION OF TRIFLUOROETHYL SULFIDE

Anodic methoxylation and acetoxylation of phenyl trifluoroethyl sulfide were successfully performed to give the corresponding α-methoxy and α-acetoxy sulfides in good to excellent yields, respectively.These products were found to be useful building blocks

16-Substituted prostaglandins

A process for producing optically active 16-substituted prostaglandins and new 16-substituted prostaglandins produced thereby which are useful as cardiovascular agents and as agents for inducing labor in pregnant females and for the termination of pregnancy.

16-CF3 prostaglandins

A process for producing optically active 16-substituted prostaglandins and new 16-substituted prostaglandins produced thereby which are useful as cardiovascular agents and as agents for inducing labor in pregnant females and for the termination of pregnan

13,14-Dihydro-16-fluoro prostaglandin F1

Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggregation, increase of nasal patency, labor inducement at term, and wound healing.

16-Fluoro prostaglandin E1 analogs

Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggregation, increase of nasal patency, labor inducement at term, and wound healing.

13,14-Dihydro-16-fluoro prostaglandin A1 analogs

Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggregation, increase of nasal patency, labor inducement at term, and wound healing.

16-Fluoro prostaglandin F2 analogs

Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggregation, increase of nasal patency, labor inducement at term, and wound healing.

13,14-Dihydro-16-fluoro prostaglandin B1 analogs

Prostaglandin-type compounds with one or two fluoro substituents at the C-16 position are disclosed, with processes for making them. These compounds are useful for a variety of pharmacological purposes, including anti-ulcer, inhibition of platelet aggregation, increase of nasal patency, labor inducement at term, and wound healing.