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Di(o,o-di-tert-butyl-p-methyl)phenyl chlorophosphite is a complex organophosphorus compound with the chemical formula C19H29ClO3P. It is characterized by a phenyl ring with a chlorophosphite group attached to it, and two di-tert-butyl-p-methyl substituents on the ortho positions of the phenyl ring. Di(o,o-di-tert-butyl-p-methyl)phenyl chlorophosphite is known for its reactivity and is often used as a reagent in organic synthesis, particularly in the formation of phosphite esters and as a ligand in transition metal catalysis. Due to its potential reactivity and toxicity, it is important to handle this chemical with care, following appropriate safety protocols.

1436-32-4

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1436-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1436-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1436-32:
(6*1)+(5*4)+(4*3)+(3*6)+(2*3)+(1*2)=64
64 % 10 = 4
So 1436-32-4 is a valid CAS Registry Number.

1436-32-4Relevant academic research and scientific papers

CONVENIENT UNIMOLECULAR SOURCES OF ARYLOXYL RADICALS.III - PHOTOLYSIS OF BIS(ARYLOXY)PHOSPHINE AZIDES

Kalgutkar, Rajdeep,Ionkin, Alexey S.,Quin, Louis D.,Lahti, Paul M.

, p. 3889 - 3892 (2007/10/02)

Photolysis of sterically hindered bis(aryloxy)phosphine azides in solution, frozen matrix, or neat solid states leads to facile unimolecular production of aryloxyl radicals.

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