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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-Indole-2-carbonitrile, 3-methyl-

N#Cc1[nH]c2c(c1C)cccc2 Request for Quotation
Chemical Name: 1H-Indole-2-carbonitrile, 3-methyl-
CAS Number: 13006-59-2
Product Number: AG000TYK(AGN-PC-0JTGHC)
Synonyms:
MDL No:
Molecular Formula: C10H8N2
Molecular Weight: 156.1839

Identification/Properties

Computed Properties
Molecular Weight:
156.188g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
156.069g/mol
Monoisotopic Mass:
156.069g/mol
Topological Polar Surface Area:
39.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
215
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


3-Methyl-1H-indole-2-carbonitrile is a versatile compound widely used in chemical synthesis. This specific compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a key intermediate in the synthesis of diverse compounds, including indole derivatives, heterocyclic compounds, and complex organic molecules.In chemical synthesis, 3-Methyl-1H-indole-2-carbonitrile is utilized as a precursor for the construction of biologically active compounds. Its incorporation into molecular frameworks allows chemists to introduce specific functional groups and structural motifs, thereby modulating the properties and activities of the final products. By utilizing this compound as a starting material, researchers can access a wide range of chemical transformations, enabling the efficient and selective synthesis of target molecules with desired properties.Additionally, the presence of the cyano group in 3-Methyl-1H-indole-2-carbonitrile imparts valuable synthetic utility, as it can undergo various reactions such as nucleophilic additions, substitution reactions, and transition metal-catalyzed transformations. This flexibility in chemical reactivity further enhances the applicability of this compound in the construction of complex molecular architectures.Overall, the strategic incorporation of 3-Methyl-1H-indole-2-carbonitrile in chemical synthesis allows for the efficient and tailored preparation of valuable compounds with diverse applications in the fields of pharmaceuticals, materials science, and agrochemicals.