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5-methyl-2-p-tolyl-2H-pyrazole-3-carboxylic acid ethyl ester is a complex organic compound with the molecular formula C14H16N2O2. It is characterized by a pyrazole ring, which is a five-membered aromatic ring containing two nitrogen atoms, and a carboxylic acid group. The molecule also features a methyl group and a p-tolyl group, which is a phenyl ring with a methyl substituent at the para position. The ethyl ester functional group indicates that the carboxylic acid is esterified with an ethyl group. 5-methyl-2-p-tolyl-2H-pyrazole-3-carboxylic acid ethyl ester is synthesized through a series of chemical reactions and is often used in pharmaceutical research due to its potential biological activities. It is a white crystalline solid and is soluble in organic solvents. The compound's structure and properties make it a candidate for further exploration in drug development, particularly in the areas of anti-inflammatory and analgesic effects.

2080-80-0

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2080-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2080-80-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2080-80:
(6*2)+(5*0)+(4*8)+(3*0)+(2*8)+(1*0)=60
60 % 10 = 0
So 2080-80-0 is a valid CAS Registry Number.

2080-80-0Relevant academic research and scientific papers

Microwave-assisted synthesis of tetrazolyl pyrazole amides

Hu, Jun,Wang, Jikui,Zhou, Taoyu,Xu, Yanhua

experimental part, p. 525 - 527 (2011/11/30)

A rapid and efficient microwave-assisted synthesis N-(1H-tetrazol-5-yl) derivatives of 3-methyl-1-phenyl-1H-pyrazole- 5-carboxamide is described. These tetrazole pyrazole amides have interesting bacteriocidal, pesticidal, herbicidal and antimicrobial activities. They were identified by IR and 1H NMR elemental analyses. The target compounds were obtained in a shorter reaction time compared to conventional heating methods.

Functionalized 4-aminoquinolines by rearrangement of pyrazole N-heterocyclic carbenes

Schmidt, Andreas,Muenster, Niels,Dreger, Andrij

supporting information; experimental part, p. 2790 - 2793 (2010/07/04)

(Figure Presented) Thermal decarboxylation of 1-phenyl pyrazolium-3- carboxylates from the mesomeric betaine class of substances leads to pyrazole-N-heterocyclic carbenes, which immediately rearrange to multiply substituted 4-aminoquinolines (see scheme). These species are of interest for the synthesis of heterocycles and pharmacologically active compounds.

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