118642-72-1 Usage
Description
2-Benzyl-4,4,4-trifluoro-3-oxobutyric acid ethyl ester is a synthetic organic compound with the molecular formula C15H13F3O3. It is a derivative of 3-oxobutyric acid and is commonly used in the production of pharmaceuticals and agrochemicals. 2-BENZYL-4,4,4-TRIFLUORO-3-OXOBUTYRIC ACID ETHYL ESTER is known for its potential use as a building block in the synthesis of complex organic molecules, making it a valuable intermediate in various chemical reactions.
Uses
Used in Pharmaceutical Industry:
2-Benzyl-4,4,4-trifluoro-3-oxobutyric acid ethyl ester is used as an intermediate in the synthesis of various pharmaceutical compounds. Its versatile chemical properties allow it to be incorporated into the development of new drugs and medications, contributing to advancements in healthcare and medicine.
Used in Agrochemical Industry:
In the agrochemical industry, 2-benzyl-4,4,4-trifluoro-3-oxobutyric acid ethyl ester is utilized as a key component in the production of pesticides and other agricultural chemicals. Its role in these applications helps to improve crop protection and contribute to more efficient and sustainable agricultural practices.
Used as a Building Block in Organic Synthesis:
2-Benzyl-4,4,4-trifluoro-3-oxobutyric acid ethyl ester is also used as a building block in the synthesis of complex organic molecules. Its unique structure and properties make it a sought-after compound for researchers and chemists working on the development of new organic compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 118642-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,4 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118642-72:
(8*1)+(7*1)+(6*8)+(5*6)+(4*4)+(3*2)+(2*7)+(1*2)=131
131 % 10 = 1
So 118642-72-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H13F3O3/c1-2-19-12(18)10(11(17)13(14,15)16)8-9-6-4-3-5-7-9/h3-7,10H,2,8H2,1H3
118642-72-1Relevant articles and documents
Studies on New Acidic Azoles as Glucose-Lowering Agents in Obese, Diabetic db/db Mice
Kees, Kenneth L.,Caggiano, Thomas J.,Steiner, Kurt E.,Fitzgerald, John J.,Kates, Michael J.,et al.
, p. 617 - 628 (1995)
Bioisosteric substitution was used as a tool to generate several new structural alternatives to the thiazolidine-2,4-dione and tetrazole heterocycles as potential antidiabetic agents.Among the initial leads that emerged from this strategy, a family of aci
Deacylative oxidation strategy for the preparation of α- functionalized carbonyls
Brodsky, Benjamin H.,Du Bois
, p. 2619 - 2621 (2007/10/03)
(Matrix Presented) α-Alkoxylation and amination of carbonyl derivatives is made possible through a unique deacylative coupling reaction that proceeds via in situ Rh-carbene formation and subsequent heteroatom-H (X-H) insertion. Reactions perform optimally
Alkylation of Ethyl 4,4,4-Trifluoroacetoacetate. First Example of a Reversible O-Alkylation Process leading to C-Alkylation
Begue, Jean-Pierre,Charpentier-Morize, Micheline,Nee, Gerard
, p. 83 - 84 (2007/10/02)
In aprotic polar solvents the ratio of O vs.C alkylation products of ethyl 4,4,4-trifluoroacetoacetate (ETFAA) can be dependent on reaction time; in hexamethylphosphoric triamide (HMPA) or acetone, the SN2 cleavage of enol ethers of ETFAA with sodium iodide was observed with concomitant formation of the sodium enolate and the corresponding iodides, and in the case of an activated iodide the mono- and di-alkylation products resulted quantitavely.