924862-20-4 Usage
Uses
Used in Chemical Research and Synthesis:
Methyl 2-ethylbenzo[d]oxazole-5-carboxylate is used as a precursor in chemical research and synthesis for its unique structural properties and reactivity, making it a useful building block for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
Methyl 2-ethylbenzo[d]oxazole-5-carboxylate is used as a potential component in the development of new drugs due to its unique structural properties and reactivity, which can contribute to the creation of novel therapeutic agents.
It is important to handle Methyl 2-ethylbenzo[d]oxazole-5-carboxylate with caution as it may pose certain hazards if mishandled.
Check Digit Verification of cas no
The CAS Registry Mumber 924862-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,8,6 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 924862-20:
(8*9)+(7*2)+(6*4)+(5*8)+(4*6)+(3*2)+(2*2)+(1*0)=184
184 % 10 = 4
So 924862-20-4 is a valid CAS Registry Number.
924862-20-4Relevant academic research and scientific papers
PYRAZOLOPYRIDINE PYRAZOLOPYRIMIDINE AND RELATED COMPOUNDS
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Paragraph 1176; 1177, (2015/11/25)
In one aspect this invention relates generally to compounds of Formula: and sub-formulas thereof, or a tautomer of each thereof, a pharmaceutically acceptable salt of each thereof, or a pharmaceutically acceptable solvate of each of the foregoing, where X1, L1, L3, and R3 are described herein.
Synthesis of some novel 2-substituted-N-aryl-benzoxazole-5-carboxamides using cobalt dipyridine dichloride as a catalyst
Sarangapani,Sridhar,Arjun,Adharvana Chari
, p. 1187 - 1190 (2008/12/20)
(Chemical Equation Presented) An efficient synthesis of some novel 2-substituted-N-aryl-benzoxazole-5-carboxamides from 2-substituted - 5-carbomethoxy benzoxazole on treatment with different substituted anilines promoted by cobalt dipyridine dichloride as a catalyst is described. This new approach has the advantage of excellent yields (90%) and short reaction times 1-2 h.