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2-(trifluoromethyl)dibenzo[b,d]thiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

177586-39-9

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177586-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177586-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,5,8 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 177586-39:
(8*1)+(7*7)+(6*7)+(5*5)+(4*8)+(3*6)+(2*3)+(1*9)=189
189 % 10 = 9
So 177586-39-9 is a valid CAS Registry Number.

177586-39-9Downstream Products

177586-39-9Relevant academic research and scientific papers

Nickel-Mediated Trifluoromethylation of Phenol Derivatives by Aryl C?O Bond Activation

Hu, Wei-Qiang,Pan, Shen,Qing, Feng-Ling,Vicic, David A.,Xu, Xiu-Hua

, p. 16076 - 16082 (2020/07/04)

The increasing pharmaceutical importance of trifluoromethylarenes has stimulated the development of more efficient trifluoromethylation reactions. Tremendous efforts have focused on copper- and palladium-mediated/catalyzed trifluoromethylation of aryl halides. In contrast, no general method exists for the conversion of widely available inert electrophiles, such as phenol derivatives, into the corresponding trifluoromethylated arenes. Reported herein is a practical nickel-mediated trifluoromethylation of phenol derivatives with readily available trimethyl(trifluoromethyl)silane (TMSCF3). The strategy relies on PMe3-promoted oxidative addition and transmetalation, and CCl3CN-induced reductive elimination. The broad utility of this transformation has been demonstrated through the direct incorporation of trifluoromethyl into aromatic and heteroaromatic systems, including biorelevant compounds.

Direct C-H Trifluoromethylation of Glycals by Photoredox Catalysis

Wang, Bang,Xiong, De-Cai,Ye, Xin-Shan

supporting information, p. 5698 - 5701 (2015/12/01)

A mild, efficient, and practical transformation for the direct C-H trifluoromethylation of glycals under visible light has been reported for the first time. This reaction employed fac-Ir3+(ppy)3 as the photocatalyst, Umemoto's reagent as the CF3 source, and a household blue LED or sunlight as the light source. Glycals bearing both electron-withdrawing and -donating protective groups performed this reaction smoothly. This visible light-mediated trifluoromethylation reaction was highlighted by the trifluoromethylation of the biologically important Neu2en moiety.

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