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1,1,1-Trifluoro-2,2-bis(p-tolyl)ethane is an organic compound characterized by its unique molecular structure. It consists of an ethane backbone with two p-tolyl groups (each containing a para-methylphenyl ring) attached to the central carbon atoms. The molecule also features a trifluoromethyl group (-CF3) attached to the same carbon as the p-tolyl groups. 1,1,1-trifluoro-2,2-bis(p-tolyl)ethane is known for its potential applications in various chemical and pharmaceutical industries, as well as its unique properties such as its lipophilicity and stability. Due to its complex structure, it is often synthesized through multi-step processes and can be used as a building block for more complex molecules or as a solvent in certain chemical reactions.

384-95-2

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384-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 384-95-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 384-95:
(5*3)+(4*8)+(3*4)+(2*9)+(1*5)=82
82 % 10 = 2
So 384-95-2 is a valid CAS Registry Number.

384-95-2Downstream Products

384-95-2Relevant academic research and scientific papers

Fluoroanalogs of DDT: Superacidic BF3-H2O catalyzed facile synthesis of 1,1,1-trifluoro-2,2-diarylethanes and 1,1-difluoro-2,2- diarylethanes

Prakash, G. K. Surya,Paknia, Farzaneh,Mathew, Thomas,Mloston, Gzregorz,Joschek, Jens P.,Olah, George A.

supporting information; experimental part, p. 4128 - 4131 (2011/10/04)

The one-pot synthesis of 1,1,1-trifluoro- and 1,1-difluoro-2,2- diarylethanes from arenes and fluorinated hemiacetals in the BF 3-H2O system is described. The reaction is simple, clean, and convenient, eliminating the use of organic

Condensations of aryl trifluoromethyl ketones with arenes in acidic media

O'Connor, Matthew J.,Boblak, Kenneth N.,Spitzer, Ashley D.,Gucciardo, Peter A.,Baumann, Andrew M.,Peter, Joshua W.,Chen, Connie Y.,Peter, Ronald,Mitton, Adam A.,Klumpp, Douglas A.

scheme or table, p. 4984 - 4987 (2011/02/21)

The chemistry of trifluoromethyl ketones has been studied. The work examines the condensation reactions of trifluoromethyl ketones with arenes in the superacid, including both synthetic and mechanistic aspects.

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