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phenyldimethylacetyl radical is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84175-26-8

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84175-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84175-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,7 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84175-26:
(7*8)+(6*4)+(5*1)+(4*7)+(3*5)+(2*2)+(1*6)=138
138 % 10 = 8
So 84175-26-8 is a valid CAS Registry Number.

84175-26-8Downstream Products

84175-26-8Relevant academic research and scientific papers

Absolute Rate Constants for Decarbonylation of Phenylacetyl and Related Radicals

Turro, Nicholas J.,Gould, Ian R.,Baretz, Bruce H.

, p. 531 - 532 (1983)

The rate constants and Arrhenius parameters for decarbonylation of phenylacetyl (C6H5CH2CO), phenylmethylacetyl (C6H5CHCH3CO), and phenyldimethylacetyl radicals in isooctane have been determined by laser flash photolysis.The variation of the rate constant for decarbonylation follows the pattern expected from radical stabilities, but the activation energies do not.It is proposed that previously unrecognized conformational restrictions may be significant in determinig decarbonylation rates.

Primary Processes in the Type I Photocleavage of Dibenzyl Ketones. A Pulsed Laser and Photochemically Induced Dynamic Nuclear Polarization Study

Gould, Ian R.,Baretz, Bruce H.,Turro, Nicholas J.

, p. 925 - 929 (2007/10/02)

The primary homolytic α-cleavage, and subsequent decarbonylation of the intermediate phenacyl radicals, have been studied for the type I photoreaction of a series of dibenzyl ketones, using the techiques of pulsed laser photolysis and photochemically induced dynamic nuclear polarization (photo-CIDNP).Evidence for selective primary cleavage to produce the most stable radical pairs is obtained for unsymmetrical ketones.The absolute rate constants and activation parameters for the decarboxylations are obtained, and the relationships between these and the stabilities of the product radicals is discussed.

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