5-Chloro-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehyde – 95%, high purity , CAS No.947-95-5

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Sku: 1759821491-5335
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Pubchem Sid488190738 Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488190738 Canonical SmilesCC1=NN(C(=C1C=O)Cl)C2=CC=CC=C2 IUPAC Name5-chloro-3-methyl-1-phenylpyrazole-4-carbaldehyde InChIKeyDKZPJLZXLKAMDO-UHFFFAOYSA-N INCHI1S/C11H9ClN2O/c1-8-10(7-15)11(12)14(13-8)9-5-3-2-4-6-9/h2-7H,1H3 Isomeric SMILES CC1=NN(C(=C1C=O)Cl)C2=CC=CC=C2 Molecular Weight 220.66 Reaxy-Rn 167848 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=167848&ln=
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Description

5-Chloro-3-methyl-1-phenyl-4-pyrazolecarboxaldehyde (5-Chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde) can be synthesized from 3-methyl-1-phenyl-1Hpyrazol-5(4H)-one under Vilsmeier-Haack reaction conditions. Knoevenagel condensation of 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde with ethylcyanoacetate at 0?C has been reported to afford ethyl-2-cyano-3-(5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-yl)propionate. It participates in the synthesis of 2-((5-phenoxy-3-methyl-1-phenyl-1H-pyrazol- 4-yl)methylene)hydrazinecarbothiomide derivatives with a potential anticonvulsant property.

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