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3,4'-bis(trifluoromethyl)-1,1'-biphenyl is an organic compound with the molecular formula C14H8F6. It is a derivative of biphenyl, featuring two trifluoromethyl groups (-CF3) attached to the 3 and 4' positions of the biphenyl core. 3,4'-bis(trifluoromethyl)-1,1'-biphenyl is characterized by its symmetrical structure and strong electron-withdrawing properties due to the presence of fluorine atoms. It is often used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. The compound is known for its stability and can be synthesized through various methods, including Friedel-Crafts acylation and nucleophilic substitution reactions. Its applications span across different industries, highlighting its versatility in chemical research and development.

2369-74-6

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2369-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2369-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2369-74:
(6*2)+(5*3)+(4*6)+(3*9)+(2*7)+(1*4)=96
96 % 10 = 6
So 2369-74-6 is a valid CAS Registry Number.

2369-74-6Downstream Products

2369-74-6Relevant articles and documents

Nickel/magnesium-lanthanum mixed oxide catalyst in the Kumada-coupling

Kiss, Arpad,Hell, Zoltan,Balint, Maria

, p. 331 - 335 (2010)

A new, heterogeneous, magnesium-lanthanum mixed oxide solid base-supported nickel(ii) catalyst was developed. The catalyst was used successfully in the Kumada coupling of aryl halides, especially aryl bromides. The optimal reaction conditions of the coupling were determined.

Palladium(II)-catalyzed coupling of electron-deficient arenes via C-H activation

Zhou, Lihong,Lu, Wenjun

scheme or table, p. 2124 - 2127 (2012/06/01)

Homocoupling and cross-coupling of electron-deficient arenes, including nitrobenzene, (trifluoromethyl)benzene, ethyl benzoate, etc., have been developed to afford biaryls using a catalytic system of Pd(OAc) 2/trifluoroacetic acid (TFA)/O2 or K2S 2O8. The crucial step is to tune the concentrations of arenes and the loading of TFA carefully to enhance the reaction rates and the selectivity of these couplings involving dual C-H activation.

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