369631-83-4 Usage
Uses
Used in Pharmaceutical Industry:
Ethyl 2-(5-Methyl-2-phenyloxazol-4-yl)acetate is used as an active pharmaceutical ingredient for its potential medicinal properties. It contributes to the development of new drugs and therapies, enhancing their efficacy and safety.
Used in Fragrance Industry:
In the fragrance industry, ethyl 2-(5-Methyl-2-phenyloxazol-4-yl)acetate is used as a scent component for its pleasant aroma. It adds a unique and appealing scent to perfumes, colognes, and other fragrance products, enhancing their overall appeal and attractiveness.
Used in Flavoring Industry:
Ethyl 2-(5-Methyl-2-phenyloxazol-4-yl)acetate is also used as a flavoring agent in the food and beverage industry. Its pleasant taste and aroma enhance the flavor profiles of various products, making them more enjoyable and palatable for consumers.
Used in Organic Synthesis and Chemical Research:
As a building block in organic synthesis, ethyl 2-(5-Methyl-2-phenyloxazol-4-yl)acetate is utilized in the development of new chemical compounds and materials. It serves as a valuable intermediate in the synthesis of complex organic molecules, contributing to advancements in chemical research and innovation.
The exact properties and applications of ethyl 2-(5-Methyl-2-phenyloxazol-4-yl)acetate may vary depending on its specific formulation and intended use, making it a versatile and valuable compound across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 369631-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,9,6,3 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 369631-83:
(8*3)+(7*6)+(6*9)+(5*6)+(4*3)+(3*1)+(2*8)+(1*3)=184
184 % 10 = 4
So 369631-83-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO3/c1-3-17-13(16)9-12-10(2)18-14(15-12)11-7-5-4-6-8-11/h4-8H,3,9H2,1-2H3
369631-83-4Relevant academic research and scientific papers
A two-step, one-pot procedure using acid chlorides and propargyl amines to form tri-substituted oxazoles via gold-catalyzed cyclization
Tran-Dubé, Michelle,Johnson, Sarah,McAlpine, Indrawan
, p. 259 - 261 (2013/02/23)
2,4-Disubstituted-5-methyl oxazoles were prepared from a 2-step, 1-pot procedure using acid chlorides and propargyl amines. These conditions lead to the formation of propargyl amides in situ followed by AuCl3 catalyzed cyclization. We were inte
Synthesis of 2,4,5-Trisubstituted Oxazoles
Cai, Xiao-hua,Yang, Hai-jun,Zhang, Guo-lin
, p. 1569 - 1571 (2007/10/03)
2,4,5-Trisubstituted oxazoles were synthesized in good yields starting from α-methylene ketones by nitrosation, condensation with aldehydes and reduction with zinc in acetic acid at 40 deg C. (5-Methyl-2-phenyloxazol-4-yl)ethanol was prepared by reduction of ethyl (5-methyl-2-phenyloxazol-4-yl)acetate with LiAlH4.
