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TCI

CAS 13024-90-3

1-(4-Chlorophenyl)-3-methyl-5-pyrazolone TCI C0953

1-(4-Chlorophenyl)-3-methyl-5-pyrazolone TCI C0953

Chemical Identity

CAS No.
13024-90-3
PubChem
CID 83055·SID 87565999
Formula
C10H9ClN2O
Molecular weight
208.65 g/mol
Purity
>98.0%(T)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(4-chlorophenyl)-5-methyl-4H-pyrazol-3-one
SMILES
CC1=NN(C(=O)C1)C2=CC=C(C=C2)Cl
InChIKey
WHIXQFSPEDIMGL-UHFFFAOYSA-N
MDL
MDL00043814
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TCI C0953 1-(4-Chlorophenyl)-3-methyl-5-pyrazolone (CAS 13024-90-3) is a heterocyclic pyrazolone building block carrying a 4-chlorophenyl substituent on the ring nitrogen. Its reactive ring carbon makes it a classic coupling component for azo dye and pigment synthesis, as well as a starting point for condensation reactions with aldehydes. Pyrazolone scaffolds are also widely explored in medicinal chemistry and as ligands for metal complexation. Offered in 25 g and 500 g packs, the solid should be kept tightly closed in a cool, dry, light-protected place.

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  • Dacre et al. (1993). p-Chlorophenyl Methyl Sulfide, p-Chlorophenyl Methyl Sulfoxide, and p-Chlorophenyl Methyl Sulfone. III. Toxicokinetics and Metabolism in Rats and Rhesus Monkeys. Journal of the American College of Toxicology doi:10.1177/109158189301200409
  • Thake et al. (1993). p-Chlorophenyl Methyl Sulfide, p-Chlorophenyl Methyl Sulfoxide, and p-Chlorophenyl Methyl Sulfone. II. Subchronic Effects in Rodents and Rhesus Monkeys. Journal of the American College of Toxicology doi:10.1177/109158189301200408
  • Leber et al. (1993). p-Chlorophenyl Methyl Sulfide, p-Chlorophenyl Methyl Sulfoxide, and p-Chlorophenyl Methyl Sulfone. I. Acute Toxicity and Bacterial Mutagenicity Studies. Journal of the American College of Toxicology doi:10.1177/109158189301200407

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.