33142-24-4 Usage
Uses
Used in Pharmaceutical Synthesis:
2-FORMYL-3-OXO-BUTYRIC ACID ETHYL ESTER is used as a reagent in the pharmaceutical industry for the synthesis of various organic compounds and pharmaceuticals. Its unique chemical structure makes it a valuable component in the creation of new drugs and medicinal agents.
Used in Perfumery:
2-FORMYL-3-OXO-BUTYRIC ACID ETHYL ESTER is used as a fragrance ingredient in the perfumery industry. Its fruity and floral scent contributes to the development of various perfumes and scented products, enhancing their appeal and sensory experience.
Used in Flavorings:
In the flavoring industry, 2-FORMYL-3-OXO-BUTYRIC ACID ETHYL ESTER is used as a flavoring agent to impart a pleasant taste to food products. Its ability to add a unique flavor profile makes it a sought-after ingredient in the development of food and beverage formulations.
Used in the Food Industry:
2-FORMYL-3-OXO-BUTYRIC ACID ETHYL ESTER has potential applications in the food industry as a flavoring agent. Its use can enhance the taste and aroma of various food products, providing a distinct and enjoyable flavor experience for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 33142-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,4 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33142-24:
(7*3)+(6*3)+(5*1)+(4*4)+(3*2)+(2*2)+(1*4)=74
74 % 10 = 4
So 33142-24-4 is a valid CAS Registry Number.
33142-24-4Relevant articles and documents
Asymmetric Aerobic Epoxidation of Unfunctionalized Olefins Catalyzed by Optically Active α-Alkoxycarbonyl-β-ketoiminato Manganese(III) Complexes
Mukaiyama, Teruaki,Yamada, Tohru,Nagata, Takushi,Imagawa, Kiyomi
, p. 327 - 330 (2007/10/02)
Optically active N,N'-ethylenebis(α-alkoxycarbonyl-β-ketoimine) was found to be a new class of effective ligand of manganese(III) complex catalyst for the asymmetric aerobic epoxidation of simple olefins, such as 1,2-dihydronaphthalene derivatives, to afford the corresponding optically active epoxides with good to high enantioselectivities.
