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Methyl 3-(3,5-dimethyl-1H-pyrazol-1-yl)propanoate is a chemical compound with the molecular formula C10H16N2O2. It is a derivative of propanoic acid, featuring a pyrazole ring attached to the third carbon of the propanoate chain. The pyrazole ring itself is substituted with two methyl groups at the 3 and 5 positions, and the entire structure is esterified with a methyl group at the carboxylic acid end. methyl 3-(3,5-dimethyl-1H-pyrazol-1-yl)propanoate is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as a building block for the creation of various biologically active molecules. Its structure provides a stable platform for further chemical modifications, making it a valuable intermediate in organic synthesis.

4819-19-6

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4819-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4819-19-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4819-19:
(6*4)+(5*8)+(4*1)+(3*9)+(2*1)+(1*9)=106
106 % 10 = 6
So 4819-19-6 is a valid CAS Registry Number.

4819-19-6Relevant academic research and scientific papers

Vilsmeier-Haak formylation of 3,5-dimethylpyrazoles

Attaryan,Antanosyan,Panosyan,Asratyan,Matsoyan

, p. 1817 - 1819 (2008/02/08)

Formylation of N-alkyl-3,5-dimethyl-1H-pyrazoles according to Vilsmeier-Haak led to the formation of the corresponding 4-formyl derivatives. 3,5-Dimethyl-1H-pyrazole having no substituent on the nitrogen atom failed to undergo formylation at the 4 position under analogous conditions. 3,5-Dimethyl-1H-pyrazole-4-carbaldehyde was synthesized by alkaline hydrolysis of methyl β-(4-formyl-3,5-dimethyl-1H-pyrazol-1-yl)propionate and subsequent heating of the acid thus formed.

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