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1-methyl-3-(pentafluoroethyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133512-63-7

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133512-63-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133512-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,1 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133512-63:
(8*1)+(7*3)+(6*3)+(5*5)+(4*1)+(3*2)+(2*6)+(1*3)=97
97 % 10 = 7
So 133512-63-7 is a valid CAS Registry Number.

133512-63-7Relevant academic research and scientific papers

PENTAFLUOROETHYLATING COMPOSITIONS

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Page/Page column 37; 38; 39, (2015/02/25)

The present invention relates to pentafluoroethylating compositions, processes for obtaining them, and their use in pentafluoroethylation reactions.

Pentafluoroethylating compositions

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Paragraph 0195, (2015/02/25)

The present invention relates to pentafluoroethylating compositions, processes for obtaining them, and their use in pentafluoroethylation reactions.

Cupration of C2F5H: Isolation, structure, and synthetic applications of [K(DMF)2][(t -BuO)Cu(C2F 5)]. Highly efficient pentafluoroethylation of unactivated aryl bromides

Lishchynskyi, Anton,Grushin, Vladimir V.

supporting information, p. 12584 - 12587 (2013/09/23)

Pentafluoroethane, C2F5H (HFC-125), is smoothly cuprated with preisolated or in situ-generated [K(DMF)][(t-BuO)2Cu] to give [K(DMF)2][(t-BuO)Cu(C2F5)] (1) in nearly quantitative yield. Complex 1 has been isolated, structurally characterized, and demonstrated to be an exceedingly versatile pentafluoroethylating reagent for a variety of substrates, including unactivated aryl bromides.

A NOVEL AND CONVENIENT METHOD FOR TRIFLUOROMETHYLATION OF ORGANIC HALIDES USING CF3SiR'3/KF/Cu(I) SYSTEM

Urata, Hisao,Fuchikami, Takamasa

, p. 91 - 94 (2007/10/02)

Fluoride ion induced cross-coupling reaction of organic halides with trifluoromethyltrialkylsilanes takes place in the presence of Cu(I) salts under mild reaction conditions to give the corresponding trifluoromethylated products in high yields.

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