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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-acetyl-1H-pyrazole-5-carboxylic acid

CC(=O)c1n[nH]c(c1)C(=O)O Request for Quotation
Chemical Name: 3-acetyl-1H-pyrazole-5-carboxylic acid
CAS Number: 949034-45-1
Product Number: AG0067AU(AGN-PC-015OWX)
Synonyms:
MDL No:
Molecular Formula: C6H6N2O3
Molecular Weight: 154.1234

Identification/Properties

Properties
Storage:
2-8℃;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Acetyl-1H-pyrazole-5-carboxylic acid serves as a versatile building block in chemical synthesis due to its unique structural properties and functional groups. This compound is commonly utilized in the pharmaceutical industry for the synthesis of various biologically active molecules. Its acetyl group can undergo various transformations, allowing for the introduction of different substituents at the pyrazole ring. Additionally, the carboxylic acid functionality enables the formation of amide bonds, facilitating the connection of this compound to other molecules in complex syntheses. Furthermore, the presence of the pyrazole ring imparts desirable pharmacological properties to the final products, making this compound a valuable tool in drug discovery and development.