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1,1-difluoro-2,2-bis(p-fluorophenyl)ethane is a synthetic organic compound characterized by its unique molecular structure. It consists of an ethyl group (C2H4) with two fluorine atoms attached to the terminal carbons (1,1-difluoro) and two p-fluorophenyl groups (each containing a fluorine atom attached to a phenyl ring) bonded to the central carbon atoms. 1,1-difluoro-2,2-bis(p-fluorophenyl)ethane is known for its potential applications in various chemical and pharmaceutical industries, particularly as a precursor in the synthesis of pharmaceuticals and agrochemicals. Due to its fluorinated nature, it may exhibit unique properties such as enhanced lipophilicity and metabolic stability, which can be beneficial in drug design. However, it is important to note that the specific applications and properties of 1,1-difluoro-2,2-bis(p-fluorophenyl)ethane would be subject to further research and development, as well as safety and efficacy testing.

437-42-3

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437-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 437-42-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 437-42:
(5*4)+(4*3)+(3*7)+(2*4)+(1*2)=63
63 % 10 = 3
So 437-42-3 is a valid CAS Registry Number.

437-42-3Relevant 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

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