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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-6-carbonitrile, 1-methyl-

N#Cc1ccc2c(c1)n(C)cc2 Request for Quotation
Chemical Name: 1H-Indole-6-carbonitrile, 1-methyl-
CAS Number: 20996-87-6
Product Number: AG00BC7S(AGN-PC-00P2QA)
Synonyms:
MDL No:
Molecular Formula: C10H8N2
Molecular Weight: 156.1839

Identification/Properties

Computed Properties
Molecular Weight:
156.188g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
156.069g/mol
Monoisotopic Mass:
156.069g/mol
Topological Polar Surface Area:
28.7A^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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methyl-1H-indole-6-carbonitrile is a versatile compound commonly used in chemical synthesis due to its unique properties. This molecule serves as a key building block in the manufacturing of various organic compounds, making it a valuable tool for synthetic chemists. In particular, 1-Methyl-1H-indole-6-carbonitrile is frequently employed in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its ability to participate in a wide range of reactions, such as nucleophilic substitutions, condensations, and cyclizations, allows for the efficient production of complex molecules with high purity and yield. Additionally, the presence of the carbonitrile functional group provides opportunities for further derivatization, enabling the creation of diverse chemical structures for various applications in the fields of medicine, materials science, and more. By incorporating 1-Methyl-1H-indole-6-carbonitrile into synthetic pathways, chemists can access new avenues for developing innovative and commercially important compounds.