62457-60-7 Usage
Description
Ethyl 2-(3-oxocyclopentyl)acetate, also known as ethyl 3-oxocyclopentane-1-acetate, is a colorless liquid chemical compound with a sweet, fruity odor. It is commonly used in the fragrance and flavor industry due to its pleasant scent.
Used in Food and Beverage Industry:
Ethyl 2-(3-oxocyclopentyl)acetate is used as a flavoring agent for its sweet, fruity odor, enhancing the taste and aroma of various food and beverage products.
Used in Perfume and Personal Care Industry:
Ethyl 2-(3-oxocyclopentyl)acetate is used as a fragrance ingredient in the production of perfumes, soaps, and other personal care products, adding a pleasant scent to these products.
Used in Industrial Applications:
Ethyl 2-(3-oxocyclopentyl)acetate functions as a solvent in various industrial applications, utilizing its chemical properties for specific processes.
Check Digit Verification of cas no
The CAS Registry Mumber 62457-60-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,5 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62457-60:
(7*6)+(6*2)+(5*4)+(4*5)+(3*7)+(2*6)+(1*0)=127
127 % 10 = 7
So 62457-60-7 is a valid CAS Registry Number.
62457-60-7Relevant articles and documents
Expedient synthesis of 3-substituted cycloalkanones via a Pd-catalyzed decarboxylative protonation protocol
Kim, Se Hee,Kim, Eun Sun,Kim, Taek Hyeon,Kim, Jae Nyoung
experimental part, p. 6256 - 6260 (2010/01/11)
We developed an efficient method for the introduction of -CH2EWG moiety at the β-position of 2-cycloalken-1-ones via a Pd-catalyzed decarboxylative protonation protocol.
Unique Molecular Discrimination in Europium Complex-Catalyzed Reactions of Saturated and α,β-Unsaturated Ketones with Ketene Silyl Acetals
Hanyuda, Kiyoshi,Hirai, Kei-Ichi,Nakai, Takeshi
, p. 31 - 32 (2007/10/03)
The unique molecular discriminations are observed in the Eu(III)-catalyzed reactions of saturated ketones, α,β-enones, and α,β-ynones with ketene silyl acetals and discussed in terms of the discriminating ability of the Eu-catalyst at the complexation sta
