759-66-0 Usage
Uses
Used in Food and Beverage Industry:
2-METHYL-3-OXO-PENTANOIC ACID ETHYL ESTER is used as a flavoring agent for its distinctive fruity and sweet aroma, enhancing the taste profiles of various food and beverage products.
Used in Perfumes and Fragrances:
In the perfumery and fragrance industry, 2-METHYL-3-OXO-PENTANOIC ACID ETHYL ESTER is utilized as a fragrance component, contributing to the creation of complex and appealing scent profiles in perfumes, colognes, and other scented products.
Used in Personal Care Products:
2-METHYL-3-OXO-PENTANOIC ACID ETHYL ESTER is used as a fragrance in personal care products, such as soaps, lotions, and shampoos, to provide a pleasant and attractive scent that enhances consumer experience.
Used in the Production of Synthetic Organic Compounds:
2-METHYL-3-OXO-PENTANOIC ACID ETHYL ESTER also serves as a key intermediate in the synthesis of other organic compounds, playing a crucial role in the chemical manufacturing processes for a variety of end products.
Check Digit Verification of cas no
The CAS Registry Mumber 759-66-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,5 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 759-66:
(5*7)+(4*5)+(3*9)+(2*6)+(1*6)=100
100 % 10 = 0
So 759-66-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O3/c1-4-7(9)6(3)8(10)11-5-2/h6H,4-5H2,1-3H3/t6-/m0/s1
759-66-0Relevant academic research and scientific papers
Acylations of Thiol Ester Enolate Anions
Wilson, G. Edwin,Hess, Arye
, p. 2766 - 2772 (2007/10/02)
The synthetic utility of thiol ester anions has been explored.Claisen condensations of thiol esters with isopropylmagnesium bromide base proceed in good yield.The Dieckmann reaction of diethyl thiolpimelate to form a six-membered ring proceeds in 74 percent yield, but the corresponding reaction of diethyl thioladipate to provide a five-membered ring gives only 26 percent yield.Neither alkylation of ethyl thiolacetate nor a Michael-type adduct with methyl vinyl ketone could be achieved.The mechanism of the Claisen condensation as it applies to thiol esters is discussed.
