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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

c1ncc2c(c1)[nH]nc2 Request for Quotation
Chemical Name: 1H-Pyrazolo[4,3-c]pyridine
CAS Number: 271-52-3
Product Number: AG0039W8(AGN-PC-02POTT)
Synonyms:
MDL No:
Molecular Formula: C6H5N3
Molecular Weight: 119.1240

Identification/Properties

Computed Properties
Molecular Weight:
119.127g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
119.048g/mol
Monoisotopic Mass:
119.048g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
105
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Pyrazolo[4,3-c]pyridine is a versatile compound that finds wide application in chemical synthesis, particularly in the pharmaceutical industry. Its unique structural properties make it a valuable building block for the synthesis of various biologically active molecules. This heterocyclic compound serves as a key intermediate in the production of potential drug candidates, as well as in the development of novel materials with interesting properties. Its presence in the synthesis pathway often contributes to enhancing the desired characteristics and functionalities of the final product. The utilization of 1H-Pyrazolo[4,3-c]pyridine in chemical synthesis showcases its significance in advancing the field of medicinal chemistry and material science.