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(3-fluorophenyl)diphenylmethane is an organic compound with the molecular formula C19H15F. It is a derivative of diphenylmethane, featuring a fluorine atom attached to the 3-position of the phenyl ring. (3-fluorophenyl)diphenylmethane is characterized by its aromatic structure, with three phenyl groups attached to a central carbon atom. The presence of the fluorine atom introduces unique electronic and steric properties, which can significantly alter the compound's reactivity and physical characteristics compared to its non-fluorinated analogs. (3-fluorophenyl)diphenylmethane is often used in the synthesis of more complex organic molecules and as a building block in pharmaceuticals and materials science due to its potential to influence the properties of the final products through its electron-withdrawing and steric effects.

1544-12-3

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1544-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1544-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,4 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1544-12:
(6*1)+(5*5)+(4*4)+(3*4)+(2*1)+(1*2)=63
63 % 10 = 3
So 1544-12-3 is a valid CAS Registry Number.

1544-12-3Downstream Products

1544-12-3Relevant academic research and scientific papers

Towards a comprehensive hydride donor ability scale

Horn, Markus,Schappele, Ludwig H.,Lang-Wittkowski, Gabriele,Mayr, Herbert,Ofial, Armin R.

supporting information, p. 249 - 263 (2013/02/25)

Rates of hydride transfer from several hydride donors to benzhydrylium ions have been measured at 20 °C and used for the determination of empirical nucleophilicity parameters N and sN according to the linear free energy relationship log k20 °C=sN(N+E). Comparison of the rate constants of hydride abstraction by tritylium ions with those calculated from the reactivity parameters sN, N, and E showed fair agreement. Therefore, it was possible to convert the large number of literature data on hydride abstraction by tritylium ions into N and sN parameters for the corresponding hydride donors, and construct a reactivity scale for hydride donors covering more than 20 orders of magnitude.

The Reduction of Fluorine-containing Triarylmethanols by Formic Acid

Andrews, Adrian F.,Mackie, Raymond K.,Walton, John C.

, p. 96 - 102 (2007/10/02)

Triarylmethanols containing one or more fluorine substituents in the para-positions are converted by 90 percent formic acid into a mixture of the fluorine-containing triarylmethane, and a second component in which one fluorine has been replaced by a hydro

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