52298-33-6 Usage
Chemical Class
Esters
Formation
Reaction between 1-ethoxy-1-oxopropan-2-ol and benzoic acid
Common Uses
Production of fragrances, flavors, solvent in various industries, component in personal care products (perfumes, lotions, soaps), pharmaceuticals, and as a reagent in organic synthesis
Safety Precautions
Handle with care, follow safety guidelines due to potential health hazards and flammability.
Check Digit Verification of cas no
The CAS Registry Mumber 52298-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,9 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52298-33:
(7*5)+(6*2)+(5*2)+(4*9)+(3*8)+(2*3)+(1*3)=126
126 % 10 = 6
So 52298-33-6 is a valid CAS Registry Number.
52298-33-6Relevant articles and documents
The role of acyloxyphosphonium ions and the stereochemical influence of base in the phosphorane-mediated esterification of alcohols
McNulty, James,Capretta, Alfredo,Laritchev, Vladimir,Dyck, Jeff,Robertson, Al J.
, p. 4051 - 4054 (2007/10/03)
Intimate details of the Mitsunobu mechanism: The trapping of an acyloxytributylphosphonium ion with a chiral secondary alcohol leads to either retention or inversion of stereochemistry in the resulting ester depending on the exclusion or inclusion of a base (see scheme). Insight into the mechanism of phosphorane-mediated esterification processes is presented.
A New Convenient Method for Esterification Using the Ph3P/CCl4 System
Ramaiah, Muthyala
, p. 4991 - 4993 (2007/10/02)
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