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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)-

1H-Pyrazolo[4,3-c]pyridine-3-carboxylicacid

OC(=O)c1n[nH]c2c1cncc2 Request for Quotation
Chemical Name: 1H-Pyrazolo[4,3-c]pyridine-3-carboxylicacid
CAS Number: 932702-11-9
Product Number: AG00H020(AGN-PC-080U2Z)
Synonyms:
MDL No:
Molecular Formula: C7H5N3O2
Molecular Weight: 163.1335

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Pyrazolo[4,3-c]pyridine-3-carboxylic acid is a versatile chemical compound that plays a crucial role in chemical synthesis processes. This compound is widely used as a building block in the creation of diverse organic molecules due to its unique structure and reactivity.In chemical synthesis, 1H-Pyrazolo[4,3-c]pyridine-3-carboxylic acid serves as a key intermediate for the formation of various heterocyclic compounds, pharmaceuticals, and agrochemicals. Its functional groups and structural features make it an essential component in the development of new materials and compounds with tailored properties.The presence of the pyrazole and pyridine rings in its structure enables 1H-Pyrazolo[4,3-c]pyridine-3-carboxylic acid to participate in various important reactions such as cyclization, functional group transformations, and cross-coupling reactions. This compound acts as a valuable scaffold for diversification and modification, allowing chemists to access a wide range of chemical space and molecular structures.Furthermore, the carboxylic acid group in 1H-Pyrazolo[4,3-c]pyridine-3-carboxylic acid provides sites for further derivatization and attachment to other molecules, facilitating the construction of complex organic frameworks and the synthesis of target compounds with specific biological or physical properties. Its versatility and synthetic utility make it a valuable tool in the hands of chemists for the development of novel compounds and materials for various applications.