53608-81-4 Usage
Uses
Used in Flavoring and Fragrance Industry:
Ethyl-2,4-diphenylbutanoate is used as a flavoring agent and fragrance for its distinctive sweet, fruity scent, enhancing the sensory appeal of products such as perfumes, soaps, and other cosmetics.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Ethyl-2,4-diphenylbutanoate serves as a valuable component in the manufacturing process of various medications, contributing to the development of new drugs and therapies.
Used in Organic Synthesis:
As a precursor in organic synthesis reactions, Ethyl-2,4-diphenylbutanoate plays a crucial role in the creation of a range of chemical compounds, facilitating advancements in the field of chemistry.
Regulatory Considerations:
Ethyl-2,4-diphenylbutanoate is considered safe for use in its various applications and is subject to regulation by governmental agencies. These regulations ensure the safety and proper handling of the compound across different industries, safeguarding both consumers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 53608-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53608-81:
(7*5)+(6*3)+(5*6)+(4*0)+(3*8)+(2*8)+(1*1)=124
124 % 10 = 4
So 53608-81-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H20O2/c1-2-20-18(19)17(16-11-7-4-8-12-16)14-13-15-9-5-3-6-10-15/h3-12,17H,2,13-14H2,1H3
53608-81-4Relevant academic research and scientific papers
Deoxygenative α-alkylation and α-arylation of 1,2-dicarbonyls
Arman, Hadi D.,Dang, Hang T.,Haug, Graham C.,Jin, Shengfei,Larionov, Oleg V.,Nguyen, Viet D.
, p. 9101 - 9108 (2020/09/17)
Construction of C-C bonds at the α-carbon is a challenging but synthetically indispensable approach to α-branched carbonyl motifs that are widely represented among drugs, natural products, and synthetic intermediates. Here, we describe a simple approach to generation of boron enolates in the absence of strong bases that allows for introduction of both α-alkyl and α-aryl groups in a reaction of readily accessible 1,2-dicarbonyls and organoboranes. Obviation of unselective, strongly basic and nucleophilic reagents permits carrying out the reaction in the presence of electrophiles that intercept the intermediate boron enolates, resulting in two new α-C-C bonds in a tricomponent process. This journal is
