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4-ethyl-4-methyl-2-phenyl-4H-oxazol-5-one is a chemical compound belonging to the oxazolone class, characterized by a five-membered oxazole ring fused with a lactone group. It features an ethyl group at the 4-position, a methyl group at the 4-position, and a phenyl group at the 2-position. 4-ethyl-4-methyl-2-phenyl-4H-oxazol-5-one is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as in the development of materials science. Its unique structure allows for various chemical reactions and modifications, making it a versatile building block in organic chemistry.

2576-61-6

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2576-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2576-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,7 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2576-61:
(6*2)+(5*5)+(4*7)+(3*6)+(2*6)+(1*1)=96
96 % 10 = 6
So 2576-61-6 is a valid CAS Registry Number.

2576-61-6Relevant academic research and scientific papers

BEMP-promoted C(4)-alkylation of 4-alkyloxazol-5(4 H)-ones: A rapid and efficient route to α,α-dialkyl-α-amino acids

Lee, Yeon-Ju,Seo, Jeyoung,Kim, Dong-Guk,Park, Hyeung-Geun,Jeong, Byeong-Seon

, p. 701 - 704 (2013/05/09)

Rapid and efficient C(4)-alkylation of 4-alkyloxazol-5(4H)-ones has been achieved by the utilization of BEMP as base. 4,4-Dialkyloxazol-5(4H)-ones, which can easily be hydrolyzed into free α,α-dialkyl-α-amino acids, were obtained in high yields (up to 99%

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