60872-11-9 Usage
Molecular weight
295.34 g/mol
Structure
A pyrazole ring with a carboxylic acid group, a butoxy group, and a phenyl group attached to the 3, 5, and 1 positions, respectively, and an ethyl ester group attached to the carboxylic acid.
Synthesis
Reacting 5-butoxy-1-phenyl-1H-pyrazole-3-carboxylic acid with ethyl iodide in the presence of a base.
Applications
Potential use in pharmaceuticals, agrochemicals, and materials science.
Unique features
Has both a carboxylic acid and an ester functional group, which may contribute to its biological activity and potential for use in the synthesis of more complex molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 60872-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,7 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60872-11:
(7*6)+(6*0)+(5*8)+(4*7)+(3*2)+(2*1)+(1*1)=119
119 % 10 = 9
So 60872-11-9 is a valid CAS Registry Number.
60872-11-9Relevant articles and documents
Synthesis and antiinflammatory and hypnotic activity of 5-alkoxy-3-(N-substituted carbamoyl)-1-phenylpyrazoles.
Sugiura,Ohno,Ohtani,Izumi,Kitamikado,Asai,Kato
, p. 80 - 85 (2007/10/08)
5-Alkoxy-3-(N-substituted carbamoly)-1-phenylpyrazoles were prepared and tested for antiinflammatory and hypnotic activity. Four compounds showed antiinflammatory activity and three possessed hypnotic properties.
