369631-83-4 Usage
General Description
Ethyl 2-(5-Methyl-2-phenyloxazol-4-yl)acetate is a chemical compound with the molecular formula C13H13NO3. It is an ester derived from oxazol and acetic acid, characterized by the presence of an ethyl group attached to a 2-(5-methyl-2-phenyloxazol-4-yl) group. ethyl 2-(5-Methyl-2-phenyloxazol-4-yl)acetate is commonly used in the production of pharmaceuticals, fragrances, and flavorings due to its pleasant aroma and potential medicinal properties. It may also be utilized as a building block in organic synthesis and chemical research. 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.
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 articles and documents
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
