631-23-2 Usage
Uses
Used in Pharmaceutical Industry:
Diethyl bis(hydroxymethyl)malonate is utilized as a synthetic intermediate for the preparation of complex molecules with potential therapeutic applications. Its reactivity with nucleophiles allows for the creation of a broad spectrum of functionalized derivatives, contributing to the development of new drugs with enhanced efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, Diethyl bis(hydroxymethyl)malonate is employed as a building block for the synthesis of various agrochemicals, including pesticides and herbicides. Its ability to form a wide range of functionalized derivatives enables the design of innovative compounds with improved performance and selectivity in agricultural applications.
Used in Organic Synthesis:
Diethyl bis(hydroxymethyl)malonate is used as a versatile reagent in organic synthesis for the preparation of complex organic molecules. Its unique structure and reactivity make it a valuable tool for chemists to construct diverse molecular architectures with potential applications in various fields, such as materials science, catalysis, and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 631-23-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 631-23:
(5*6)+(4*3)+(3*1)+(2*2)+(1*3)=52
52 % 10 = 2
So 631-23-2 is a valid CAS Registry Number.
631-23-2Relevant academic research and scientific papers
Facile synthesis of 1,2,3-tricarbonyls from 1,3-dicarbonyls mediated by cerium(IV) ammonium nitrate
Sivan, Akhil,Deepthi, Ani
supporting information, p. 1890 - 1893 (2014/03/21)
A mild and efficient protocol for the synthesis of vicinal tricarbonyl compounds from β-dicarbonyls in a single step using cerium(IV) ammonium nitrate as a catalytic oxidant is described. Ease of execution, wide substrate scope and the suitability for the synthesis of commercially important compounds like ninhydrin, alloxan and oxoline make this reaction particularly noteworthy.
