Produktname:methyl 5-(3,4-dichlorophenyl)-1H-pyrazole-3-carboxylate

IUPAC Name:methyl 5-(3,4-dichlorophenyl)-1H-pyrazole-3-carboxylate

CAS:192702-24-2
Molekulare Formel:C11H8Cl2N2O2
Reinheit:95%+
Katalognummer:CM478313
Molekulargewicht:271.1

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Produkt-Details

CAS-Nr.:192702-24-2
Molekulare Formel:C11H8Cl2N2O2
Schmelzpunkt:-
SMILES-Code:COC(=O)C1=NNC(=C1)C1=CC(Cl)=C(Cl)C=C1
Dichte:
Katalognummer:CM478313
Molekulargewicht:271.1
Siedepunkt:
Mdl-Nr.:MFCD04969778
Lagerung:

Category Infos

Pyrazoles
Pyrazoles are organic compounds of the general formula C3H3N2H. It is a five-membered heterocycle consisting of three carbon atoms and two adjacent nitrogen atoms. As an H-bond-donating heterocycle, pyrazole has been used as a more lipophilic and metabolically more stable bioisomer of phenol. Pyrazoles have attracted more and more attention due to their broad spectrum of action and strong efficacy.
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Product Other Information

Product Overview Methyl 5-(3,4-dichlorophenyl)-1H-pyrazole-3-carboxylate, also known as DCPM, is a chemical compound that has gained significant attention in scientific research due to its potential applications in various fields.
Synthesis Method Methyl 5-(3,4-dichlorophenyl)-1H-pyrazole-3-carboxylate can be synthesized using various methods, including the reaction of 3,4-dichlorophenylhydrazine with ethyl acetoacetate, followed by esterification with methanol. Another method involves the reaction of 3,4-dichlorophenylhydrazine with ethyl cyanoacetate, followed by esterification with methanol.
Synthesis and Application Methyl 5-(3,4-dichlorophenyl)-1H-pyrazole-3-carboxylate can be synthesized using various methods, including the reaction of 3,4-dichlorophenylhydrazine with ethyl acetoacetate, followed by esterification with methanol. Another method involves the reaction of 3,4-dichlorophenylhydrazine with ethyl cyanoacetate, followed by esterification with methanol.
Future Directions One area of interest is the development of more environmentally friendly pesticides that utilize methyl 5-(3,4-dichlorophenyl)-1H-pyrazole-3-carboxylate as an active ingredient. Additionally, further investigation is needed to fully understand the long-term effects of methyl 5-(3,4-dichlorophenyl)-1H-pyrazole-3-carboxylate exposure on mammals and the environment. Finally, methyl 5-(3,4-dichlorophenyl)-1H-pyrazole-3-carboxylate may have potential applications in the development of anti-inflammatory drugs for human use.