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2-(2,6-bis(trifluoromethyl)phenyl)-1,3,2-dioxaphospholane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144796-50-9

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144796-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144796-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,9 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144796-50:
(8*1)+(7*4)+(6*4)+(5*7)+(4*9)+(3*6)+(2*5)+(1*0)=159
159 % 10 = 9
So 144796-50-9 is a valid CAS Registry Number.

144796-50-9Relevant academic research and scientific papers

The molecular structure of a 2-aryl-1,3,2-dioxaphospholane and its coordination behaviour towards platinum(II) species; molecular structures of four platinum(II) complexes

Dillon, Keith B.,Goeta, Andrés E.,Monks, Philippa K.,Shepherd, Helena J.

experimental part, p. 606 - 612 (2010/06/12)

The molecular structure of the 2-aryl-1,3,2-dioxaphospholane, 2,6-(CF3)2-C6H3-P(OCH2)2 (1), has been determined by single-crystal X-ray diffraction at 120 K. Its reactions with the platinum

Metaphosphate intermediates from fluoroaromatic precursors

Chambers, Richard D.,Dillon, Keith B.,Straw, Thomas A.

, p. 385 - 388 (2007/10/02)

Flow pyrolysis of some 2-aryloxy-1,3,2-dioxaphospholanes with ortho-CF3 or F substituents, either alone or in the presence of methanol, has provided evidence for the formation of methaphosphates as intermediates; these highly reactive species then undergo further reaction, depending on the nature of the substituent.Mass spectrometric studies of the starting materials have also suggested the elimination of ethylene and the formation of methaphosphates to a limited extent.

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