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Phenol, 2-(1,1-dimethylethyl)-4-methyl-, phosphate (3:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87375-82-4

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87375-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87375-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,7 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87375-82:
(7*8)+(6*7)+(5*3)+(4*7)+(3*5)+(2*8)+(1*2)=174
174 % 10 = 4
So 87375-82-4 is a valid CAS Registry Number.

87375-82-4Downstream Products

87375-82-4Relevant academic research and scientific papers

FACTORS DETERMINING THE REACTIVITY OF PHOSPHOROUS TRIESTERS IN REACTIONS WITH CUMENE HYDROPEROXIDE

Cherkasova, O. A.,Galkin, V. I.,Sayakhov, R. D.,Mukmeneva, N. A.,Cherkasov, R. A.

, p. 862 - 865 (2007/10/02)

The kinetics of reduction of cumene hydroperoxide with a wide range of aliphatic and aromatic phosphorous triesters in benzene were studied by the polarographic method.Factors determining the reactivity of the phosphites in this reaction were investigated by the method of correlation analysis.

Syntheses und NMR-Spektren phosphororganischer Antioxidantien und verwandter Verbindungen

Koenig, T.,Habicher, W.D.,Haehner, U.,Pionteck, J.,Rueger, C.,Schwetlick, K.

, p. 333 - 349 (2007/10/02)

The syntheses of various aliphatic, aromatic, sterically hindered, and cyclic organophosphorus compounds (phosphorous acid esters, esters chlorides and ester amides, hydrogen phosphites, phosphinates and phosphates) are reported, and general procedures for preparation are given.The compounds synthesized were investigated by means of 31P-, 1H- and 13C-n.m.r. spectroscopy, and the chemical shifts measured are listed.

Organophosphorus Antioxidants. X. The Hydroperoxide Decomposing Action of Phosphites, Phosphonites and Thiophosphites

Koenig, T.,Habicher, W. D.,Schwetlick, K.

, p. 913 - 922 (2007/10/02)

The kinetics and mechanism of reactions of phosphites, phosphonites, thiophosphites and hydrogenphosphites with cumyl (CHP), t-butyl (TBHP) and α-tetralyl (THP) hydrogenperoxides has been studied by means of (31)P-n.m.r. spectroscopy, high performance liquid chromatography and iodometric titration.All three valent phosphorus compounds studied initially react with hydroperoxides stoichiometrically to give the corresponding P=O products and alcohol.Some species are able to decompose cumyl hydroperoxide catalytically to form phenol and aceton.Acyloin phosphites decompose CHP catalytically after a stoichiometric reaction as thiophosphites do.Tetramethylpiperidinyl phosphites ("HALS-phosphites") react with hydroperoxides only stoichiometrically but with high velocity.Phosphonites react with hydroperoxides in the same way as the corresponding phosphites.Their reactivity, however, is much higher.Hydrogenphosphites are less reactive than phosphites in the reaction with hydroperoxides.They are able to act catalytically.

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