1425647-31-9

Basic information

• Product Name: (Z)-1-(3,3,3-trifluoroprop-1-enyl)-3-tert-butoxycarbonylaminobenzene
• Synonyms: (Z)-1-(3,3,3-trifluoroprop-1-enyl)-3-tert-butoxycarbonylaminobenzene
• CAS NO: 1425647-31-9
• Molecular Weight: 287.282
• Mol File: 1425647-31-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (Z)-1-(3,3,3-trifluoroprop-1-enyl)-3-tert-butoxycarbonylaminobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-1-(3,3,3-trifluoroprop-1-enyl)-3-tert-butoxycarbonylaminobenzene(1425647-31-9)
• EPA Substance Registry System: (Z)-1-(3,3,3-trifluoroprop-1-enyl)-3-tert-butoxycarbonylaminobenzene(1425647-31-9)

Safety Data

• Hazardous Substances Data: 1425647-31-9(Hazardous Substances Data)

Upstream product

• 1425647-72-8 tert-butyl (E)-(3-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)phenyl)carbamate 
• 185619-66-3 (3-ethynyl-phenyl)-carbamic acid tert-butyl ester 
• 887144-94-7 Togni's reagent II 

Relevant articles and documents

Visible-light-induced synthesis of a variety of trifluoromethylated alkenes from potassium vinyltrifluoroborates by photoredox catalysis

A facile synthesis of trifluoromethylated alkenes by the radical-mediated trifluoromethylation of vinyltrifluoroborates has been developed. Togni's reagent serves as a CF3 radical precursor in the presence of the photoredox catalyst [Ru(bpy)3](PF6)2 under visible light irradiation. This new photocatalytic protocol can be applicable to a wide variety of vinylborates containing electronically diverse substituents and hetero-aromatics. The Royal Society of Chemistry 2013.