78622-55-6

Basic information

• Product Name: (E)-1-(3,3,3-trifluoroprop-1-enyl)-4-methoxybenzene
• Synonyms: (E)-1-(3,3,3-trifluoroprop-1-enyl)-4-methoxybenzene
• CAS NO: 78622-55-6
• Molecular Weight: 202.176
• Mol File: 78622-55-6.mol
• Article Data: 41

Chemical Properties

• CAS DataBase Reference: (E)-1-(3,3,3-trifluoroprop-1-enyl)-4-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(3,3,3-trifluoroprop-1-enyl)-4-methoxybenzene(78622-55-6)
• EPA Substance Registry System: (E)-1-(3,3,3-trifluoroprop-1-enyl)-4-methoxybenzene(78622-55-6)

Safety Data

• Hazardous Substances Data: 78622-55-6(Hazardous Substances Data)

Upstream product

• 887144-97-0 Togni's reagent 
• 72316-18-8 (E)-2-(4-methoxyphenyl)vinylboronic acid 
• 887144-94-7 Togni's reagent II 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 692-51-3 (E)-trimethyl(3,3,3-trifluoroprop-1-en-1-yl)silane 
• 696-62-8 para-iodoanisole 
• 1465812-79-6 2-[(2,2,2-trifluoroethyl)sulfonyl]benzo[d]thiazole 
• 123-11-5 4-methoxy-benzaldehyde 
• 830-09-1 3-(4'-methoxyphenyl)propenoic acid 
• 637-69-4 4-Methoxystyrene 
• 151-67-7 1,1,1-trifluoro-2-bromo-2-chloroethane 
• 5953-85-5 p-anisaldehyde hydrazone 
• 1214756-50-9 2-cyclopropyl-1-(trifluoromethyl)benzo[b]thiophenium triflate 
• 381-98-6 trifluoromethyacrylic acid 

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.

Reaction of substituted phenols and alcohols with (E)-1-chloro-3,3,3-trifluoropropene (HFCO-1233zd)

Simple and convenient one-pot procedures for the preparation of ArOCH=CHCF3, ROCH=CHCF3 and CF3CH=CHOArOCH = CHCF3 starting from the industrial product HFCO-1233zd (CF3CH=CHCl) are presented. These syntheses involve the reaction of 1233zd with phenols and alcohols in the presence of potassium hydroxide in DMF or pyridine solvent at elevated temperatures.

Rapid Syntheses of [11C]Arylvinyltrifluoromethanes through Treatment of (E)-Arylvinyl(phenyl)iodonium Tosylates with [11C]Trifluoromethylcopper(I)

We report a method for labeling arylvinyltrifluoromethanes with carbon-11 (t1/2 = 20.4 min) as representatives of a new radiolabeled chemotype that has potential for developing radiotracers for biomedical imaging with positron emission tomography. Treatme