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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-Indazole-6-carbonitrile

N#Cc1ccc2c(c1)[nH]nc2 Request for Quotation
Chemical Name: 1H-Indazole-6-carbonitrile
CAS Number: 141290-59-7
Product Number: AG007ZGQ(AGN-PC-0JR1HO)
Synonyms:
MDL No:
Molecular Formula: C8H5N3
Molecular Weight: 143.1454

Identification/Properties

Computed Properties
Molecular Weight:
143.149g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
143.048g/mol
Monoisotopic Mass:
143.048g/mol
Topological Polar Surface Area:
52.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
193
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-Indazole-6-carbonitrile, a versatile chemical compound, has found widespread application in organic synthesis as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials. With its unique structural properties, this compound serves as a crucial intermediate in the formation of numerous complex molecules due to its ability to undergo diverse chemical transformations. By serving as a precursor in the synthesis of heterocyclic compounds, 1H-Indazole-6-carbonitrile plays a pivotal role in the development of innovative drugs, crop protection products, and advanced materials. Its incorporation in chemical reactions facilitates the introduction of nitrile functionality into target molecules, thereby enhancing their biological activity or material properties. As a fundamental component in the toolkit of organic chemists, 1H-Indazole-6-carbonitrile contributes significantly to the advancement of chemical science and the discovery of novel compounds with diverse applications.