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2-hydroxyethyl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

851896-53-2

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851896-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851896-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,8,9 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 851896-53:
(8*8)+(7*5)+(6*1)+(5*8)+(4*9)+(3*6)+(2*5)+(1*3)=212
212 % 10 = 2
So 851896-53-2 is a valid CAS Registry Number.

851896-53-2Relevant academic research and scientific papers

Exocyclic Cleavage in the Alkaline Hydrolysis of Methyl Ethylene Phosphate: Evidence Against the Significance of Stereoelectronic Acceleration in Reactions of Cyclic Phosphates

Kluger, Ronald,Thatcher, Gregory R. J.

, p. 6006 - 6011 (1985)

The hydrolysis of methyl ethylene phosphate serves as a mechanistic probe of phosphate reactivity and as a model for enzyme catalysis.Early reports, based on proton NMR and GC analysis, indicated that observable amounts of exocyclic cleavage products are obtained in the alkaline hydrolysis reaction .However, later reports based on phosphorus NMR analysis of reactions in 5 M sodium hydroxide by advocates of a stereoelectronic theory indicated that, consistent with the theory, ring cleavage is the exclusive initial process .In the present study, the products of the reaction of methyl ethylene phosphate with hydroxide under a variety of conditions were determined by proton NMR and by phosphorus NMR with and without rapid quenching.Reactions of the products were also analyzed.The products of exocyclic cleavage, methanol and ethylene phosphate, are produced in the initial reaction to the extent that was reported in 1969.Subsequent reaction of the ring-cleaved products is too slow to account for the initial production of methanol.These data suggest that ring strain and apicophilicities of substituents, rather, than orbital interactions, account for the substantial differences in the reactivity of phosphate esters.

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