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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)-

3-Pyridinecarbonitrile, 2-(1H-imidazol-1-yl)-

N#Cc1cccnc1n1cncc1 Request for Quotation
Chemical Name: 3-Pyridinecarbonitrile, 2-(1H-imidazol-1-yl)-
CAS Number: 94448-88-1
Product Number: AG003EPB(AGN-PC-00LOKP)
Synonyms:
MDL No:
Molecular Formula: C9H6N4
Molecular Weight: 170.1707

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
170.175g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
170.059g/mol
Monoisotopic Mass:
170.059g/mol
Topological Polar Surface Area:
54.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
219
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The versatile compound 2-(1H-Imidazol-1-yl)nicotinonitrile plays a crucial role in chemical synthesis as a key intermediate. This compound is utilized in various organic reactions to introduce the imidazole and nicotinonitrile functionalities into complex molecules. Its unique structure and reactivity make it a valuable building block in the development of pharmaceuticals, agrochemicals, and materials. In organic synthesis, 2-(1H-Imidazol-1-yl)nicotinonitrile serves as a strategic component for the construction of heterocyclic frameworks and functionalized compounds with diverse applications. Its ability to undergo selective transformations enables the synthesis of novel molecules with tailored properties, making it a valuable tool for chemists in the design and preparation of advanced materials and bioactive compounds.