54897-51-7 Usage
Uses
Used in Perfumery and Fragrance Industry:
Phenyl 2-ethylbutanoate is used as a fragrance ingredient for its sweet, floral scent, contributing to the creation of perfumes, colognes, and other personal care products. Its pleasant aroma enhances the sensory experience of these products, making them more appealing to consumers.
Used in Food Industry:
In the food industry, phenyl 2-ethylbutanoate is used as a flavoring agent to impart a fruity, honey-like taste to products such as baked goods, candies, and beverages. Its ability to add a distinct flavor profile without overpowering the primary taste of the food makes it a valuable ingredient in enhancing the overall flavor experience.
Used in Industrial Applications:
Phenyl 2-ethylbutanoate can also serve as a solvent in various industrial applications. Its versatility and compatibility with different materials make it suitable for use in processes that require a solvent with specific properties, such as dissolving or diluting substances.
Check Digit Verification of cas no
The CAS Registry Mumber 54897-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54897-51:
(7*5)+(6*4)+(5*8)+(4*9)+(3*7)+(2*5)+(1*1)=167
167 % 10 = 7
So 54897-51-7 is a valid CAS Registry Number.
54897-51-7Relevant academic research and scientific papers
Direct C-C Bond Formation from Alkanes Using Ni-Photoredox Catalysis
Ackerman, Laura K. G.,Martinez Alvarado, Jesus I.,Doyle, Abigail G.
, p. 14059 - 14063 (2018/10/24)
A method for direct cross coupling between unactivated C(sp3)-H bonds and chloroformates has been accomplished via nickel and photoredox catalysis. A diverse range of feedstock chemicals, such as (a)cyclic alkanes and toluenes, along with late-stage intermediates, undergo intermolecular C-C bond formation to afford esters under mild conditions using only 3 equiv of the C-H partner. Site selectivity is predictable according to bond strength and polarity trends that are consistent with the intermediacy of a chlorine radical as the hydrogen atom-abstracting species.
