891862-16-1

Basic information

• Product Name: (1S)-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester
• Synonyms: (1S)-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester
• CAS NO: 891862-16-1
• Molecular Weight: 208.18
• Mol File: 891862-16-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1S)-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (1S)-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester(891862-16-1)
• EPA Substance Registry System: (1S)-cyclohex-3-enecarboxylic acid 2,2,2-trifluoro-ethyl ester(891862-16-1)

Safety Data

• Hazardous Substances Data: 891862-16-1(Hazardous Substances Data)

Upstream product

• 407-47-6 2,2,2-trifluoroethyl acrylate 
• 106-99-0 buta-1,3-diene 

Downstream Products

• 1423074-45-6 ethyl (cyclohex-3-enylmethyl)carbamate 
• 1423074-47-8 (1R,5S)-3-methyl-7-(pyridin-3-yl)-3-azabicyclo[3.3.1]non-6-ene p-hydroxybenzoate 
• 950690-19-4 ethyl (S)-5-((tert-butoxycarbonyl)amino)cyclohexa-1,3-diene-1-carboxylate 
• 79091-96-6 (S)-cyclohex-3-ene-1-carboxamide 

Relevant articles and documents

Development of a scalable synthesis of a pyridinyl-3-azabicyclononene, a novel nicotinic partial agonist

The process research and development of two syntheses of a novel nicotinic partial agonist, TC-8817 ((+)-5), are described. The original Medicinal Chemistry route had multiple flaws, making it unsuitable for further development. A second approach was expl

Triflimide activation of a chiral oxazaborolidine leads to a more general catalytic system for enantioselective Diels-Alder addition

The strong acid triflimide ((CF3SO2)2NH) protonates chiral oxazaborolidines to form superactive, stable, chiral Lewis acids which are highly effective catalysts for a wide variety of enantioselective Diels-Alder reactions, documented herein by more than 20 examples. Copyright