138714-53-1 Usage
Description
2,3-Dioxo-3-phenyl-propionic acid tert-butyl ester, also known as methyl 2,3-dioxo-3-phenylpropanoate, is a colorless to pale yellow liquid chemical compound with the molecular formula C13H14O4. It is primarily used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a reagent in organic synthesis and a flavoring agent in food products. Due to its potential to cause irritation to the skin, eyes, and respiratory system, it is important to handle this compound with caution and store it in a cool, dry place away from incompatible materials.
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,3-DIOXO-3-PHENYL-PROPIONIC ACID TERT-BUTYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to contribute to the formation of complex organic molecules.
Used in Organic Synthesis:
2,3-DIOXO-3-PHENYL-PROPIONIC ACID TERT-BUTYL ESTER is used as a reagent in organic synthesis for its role in facilitating chemical reactions that lead to the production of desired organic compounds.
Used in Food Industry:
2,3-DIOXO-3-PHENYL-PROPIONIC ACID TERT-BUTYL ESTER is used as a flavoring agent in food products to enhance taste and aroma, contributing to the overall sensory experience of the food items.
Check Digit Verification of cas no
The CAS Registry Mumber 138714-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,1 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138714-53:
(8*1)+(7*3)+(6*8)+(5*7)+(4*1)+(3*4)+(2*5)+(1*3)=141
141 % 10 = 1
So 138714-53-1 is a valid CAS Registry Number.
138714-53-1Relevant articles and documents
Acceleration of the Dess-Martin Oxidation by Water
Meyer, Stephanie D.,Schreiber, Stuart L.
, p. 7549 - 7552 (1994)
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SYNTHESIS AND CHARACTERIZATION OF PYRROLINONECARBOXYLATES FORMED BY REACTION OF VICINAL TRICARBONYL DERIVATIVES WITH ALDEHYDE SCHIFF BASES
Wasserman, Harry H.,Ennis, David S.,Vu, Chi B.,Schulte, Gayle,Munk, Morton E.,et al.
, p. 975 - 995 (2007/10/02)
A series of vicinal tricarbonyl derivatives undergo reaction with aldehyde Schiff bases forming pyrrolinone derivatives by benzilic acid-related rearrangements.The structures were established by X-ray analyses and, independently by the SESAMI NMR-based computer program.
BENZILIC ACID REARRANGEMENTS IN THE REACTIONS OF ARYL VICINAL TRICARBONYL DERIVATIVES WITH ALDEHYDE SCHIFF BASES
Wasserman, Harry H.,Ennis, David S.,Vu, Chi B.,Schulte, Gayle K.
, p. 6039 - 6042 (2007/10/02)
Reactions of aryl and hetero vicinal tricarbonyl derivatives with aldehyde Schiff bases of the general structure RCH2CHO lead to pyrrolinone derivatives by benzilic acid-related rearrangements, driven, most probably, by iminium ion intermediates.