509093-24-7

Upstream product

• 6776-48-3 benzyl N-(1-chloro-2,2,2-trifluoroethyl)carbamate 
• 106-95-6 allyl bromide 
• 501-53-1 benzyl chloroformate 
• 402728-74-9 N-(diphenylmethylene)-1,1,1-trifluoro-4-penten-2-amine 

Downstream Products

• 627533-03-3 benzyl N-(7-octenyl)-N-[1-(trifluoromethyl)-3-butenyl]carbamate 
• 852997-10-5 (2-bromo-allyl)-(1-trifluoromethyl-but-3-enyl)-carbamic acid benzyl ester 
• 627533-13-5 N-(benzyloxycarbonyl)-5-isopropenyl-2-(trifluoromethyl)-1,2,3,6-tetrahydropyridine 
• 627533-04-4 N-(benzyloxycarbonyl)-6-(trifluoromethyl)-1,2,5,6-tetrahydropyridine 
• 627533-09-9 benzyl N-(2-propynyl)-N-[1-(trifluoromethyl)-3-butenyl]carbamate 
• 627533-00-0 benzyl N-allyl-N-[1-(trifluoromethyl)-3-butenyl]carbamate 
• 627533-10-2 benzyl N-(2-butynyl)-N-[1-(trifluoromethyl)-3-butenyl]carbamate 
• 627533-02-2 benzyl N-(5-hexenyl)-N-[1-(trifluoromethyl)-3-butenyl]carbamate 
• 627533-01-1 benzyl N-(4-pentenyl)-N-[1-(trifluoromethyl)-3-butenyl]carbamate 

Relevant academic research and scientific papers

Synthesis of α-Trifluoromethylated Nitrogen Heterocycles

The syntheses of various α-trifluoromethylated nitrogen heterocycles have been achieved from readily available α -(trifluoromethyl)homoallylamine through a ring-closing metathesis.

Efficient syntheses of ω-trifluoromethyl substituted ω-amino acids

Syntheses of N-protected β-trifluoromethyl-β-amino acids, γ-trifluoromethyl-γ-amino acids, δ-trifluoromethyl-δ-amino acids, and β-trifluoromethyl-β-amino-α-hydroxy acids (4,4,4-trifluoroisothreonine) starting from N-acyl-1-chloro-2,2,2-trifluoroethylamines are described.