92248-58-3 Usage
Description
4-Isoxazolecarboxylic acid, 3-Methyl-5-(4-Methylphenyl)-, ethyl is a chemical compound with the molecular formula C13H13NO3. It is a derivative of isoxazolecarboxylic acid, featuring both isoxazole and carboxylic acid functional groups. The ethyl group is attached to the carboxylic acid, and the compound also contains a methyl and a 4-methylphenyl group. 4-Isoxazolecarboxylic acid, 3-Methyl-5-(4-Methylphenyl)-, ethyl may have potential applications in the pharmaceutical industry, particularly in the development of new drugs or medications. Its specific properties and uses would depend on further research and testing.
Used in Pharmaceutical Industry:
4-Isoxazolecarboxylic acid, 3-Methyl-5-(4-Methylphenyl)-, ethyl is used as a chemical intermediate for the development of new drugs or medications. Its unique structure and functional groups may contribute to the creation of innovative pharmaceutical compounds with potential therapeutic benefits. Further research and testing are required to explore its full potential and establish its specific applications in drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 92248-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,4 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92248-58:
(7*9)+(6*2)+(5*2)+(4*4)+(3*8)+(2*5)+(1*8)=143
143 % 10 = 3
So 92248-58-3 is a valid CAS Registry Number.
92248-58-3Relevant articles and documents
Palladium-Catalyzed Direct C-H Arylation of Isoxazoles at the 5-Position
Shigenobu, Masashi,Takenaka, Kazuhiro,Sasai, Hiroaki
supporting information, p. 9572 - 9576 (2015/08/11)
A palladium-catalyzed direct arylation of isoxazoles with aryl iodides has been achieved. The C-H bond at the 5-position is activated selectively to give coupling products in moderate to good yields. This direct arylation was applied to the synthesis of a spiro-type chiral ligand, which proved to be most effective to the palladium-catalyzed tandem cyclization of a dialkenyl alcohol.