1418317-24-4

Basic information

• Product Name: (E)-2-methoxy-4-(3,3,3-trifluoroprop-1-en-1-yl)phenol
• Synonyms: (E)-2-methoxy-4-(3,3,3-trifluoroprop-1-en-1-yl)phenol
• CAS NO: 1418317-24-4
• Molecular Weight: 218.175
• Mol File: 1418317-24-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-2-methoxy-4-(3,3,3-trifluoroprop-1-en-1-yl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-methoxy-4-(3,3,3-trifluoroprop-1-en-1-yl)phenol(1418317-24-4)
• EPA Substance Registry System: (E)-2-methoxy-4-(3,3,3-trifluoroprop-1-en-1-yl)phenol(1418317-24-4)

Safety Data

• Hazardous Substances Data: 1418317-24-4(Hazardous Substances Data)

Upstream product

• 1135-24-6 3-(4-hydroxy-3-methoxyphenyl)acrylic acid 
• 887144-94-7 Togni's reagent II 
• 421-83-0 trifluoromethane sulfonyl chloride 

Relevant articles and documents

Exploring the Structure and Performance of Cd–Chalcogenide Photocatalysts in Selective Trifluoromethylation

The field of heterogeneous photoredox catalysis has grown substantially and impacted organic synthesis because of the affordability and reusability of catalysts. This study reports radical trifluoromethylation with Cd–chalcogenide semiconductors. Cd semiconductors, particularly CdSe, are readily available, commercial, visible-light-responsive, heterogeneous photocatalysts. The potential of readily available Cd semiconductors, particularly CdSe, is confirmed by their increased photocatalytic activity toward trifluoromethylation with various substrates, such as (hetero)arenes and vinylic amides/acids, via addition, cyclization, and decarboxylation under visible light. The economic significance of this strategy is also highlighted through the scalable synthesis of biologically active molecules followed by catalyst reuse. Moreover, these catalysts are relatively inexpensive compared with transition metal-based homogeneous photocatalysts, presently used in organic synthesis.

Copper-and iron-catalyzed decarboxylative tri-and difluoromethylation of α,β-unsaturated carboxylic acids with CF3SO2Na and (CF2HSO2)2Zn via a radical process

A copper-catalyzed decarboxylative trifluoromethylation of various α,β-unsaturated carboxylic acids by using a stable and inexpensive solid, sodium trifluoromethanesulfinate (CF3SO2Na, Langlois reagent), was developed. In addition, an iron-catalyzed difluoromethylation of aryl-substituted acrylic acids by using zinc difluoromethanesulfinate (DFMS, (CF2HSO2)2Zn, Baran reagent) via a similar radical process was also achieved.