53841-07-9 Usage
Uses
Used in the Food and Beverage Industry:
Ethyl 3-butyonoate is used as a flavoring agent for adding a pleasant, fruity note to various food and beverage products, enhancing their overall taste and aroma.
Used in the Perfume and Fragrance Industry:
It serves as a key ingredient in the production of perfumes and other fragrance products, contributing to the creation of complex and appealing scents.
Used in the Pharmaceutical Industry:
Ethyl 3-butyonoate is utilized in the synthesis of pharmaceuticals, acting as a crucial intermediate in the development of various medicinal compounds.
Used in the Paints and Coatings Industry:
ETHYL 3-BUTYNOATE is employed as a solvent in the manufacturing of paints and coatings, improving the performance and application properties of these products.
It is important to handle ethyl 3-butyonoate with care due to its potential to irritate the eyes, skin, and respiratory system. Proper protective equipment and a well-ventilated area are essential when working with this chemical to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 53841-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,4 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53841-07:
(7*5)+(6*3)+(5*8)+(4*4)+(3*1)+(2*0)+(1*7)=119
119 % 10 = 9
So 53841-07-9 is a valid CAS Registry Number.
53841-07-9Relevant academic research and scientific papers
Formal metal-free γ-arylation of 1,3-dicarbonyl compounds: Via an isomerisation/1,4-addition/[3,3]-sigmatropic rearrangement sequence
Guan, Xi-Dong,Lu, Shi-Chao,Wen, Fu-Qiang
supporting information, p. 8964 - 8968 (2021/11/27)
A metal-free redox arylation of alkynes with sulfoxides has been developed to provide unconventional access to diverse γ-arylated 1,3-dicarbonyl compounds in an atom-economical manner. Mechanistic studies suggest that a conjugated allenone intermediate was generated in situ, which solves the problem of reactivity and regioselectivity of unsymmetrical dialkyl-substituted internal alkynes and enables the functionalisation of a broad range of substrates bearing electron-withdrawing functional groups. The resulting arylated 1,3-dicarbonyl compounds are versatile and useful building blocks for further functionalisation. This journal is
Selective one-pot synthesis of allenyl and alkynyl esters from β-ketoesters
Maity, Pradip,Lepore, Salvatore D.
supporting information; experimental part, p. 158 - 162 (2009/04/07)
(Chemical Equation Presented) A convenient method is described for the dehydration of β-ketoesters to generate conjugated and deconjugated alkynyl esters and conjugated allenyl esters. This sequential one-pot method involves the formation of a vinyl trifl
