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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)-

4-Quinolinecarbonitrile

N#Cc1ccnc2c1cccc2 Request for Quotation
Chemical Name: 4-Quinolinecarbonitrile
CAS Number: 2973-27-5
Product Number: AG002Z92(AGN-PC-0JO2I3)
Synonyms:
MDL No:
Molecular Formula: C10H6N2
Molecular Weight: 154.1680

Identification/Properties

Properties
MP:
103.5°C
BP:
243.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.4820 (estimate)
Computed Properties
Molecular Weight:
154.172g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
154.053g/mol
Monoisotopic Mass:
154.053g/mol
Topological Polar Surface Area:
36.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
203
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-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Quinoline-4-carbonitrile, also known as 4-Cyanquinoline, is a versatile compound widely used in chemical synthesis for its unique properties and reactions. This molecule serves as a valuable building block in the preparation of various complex organic compounds, making it a crucial component in synthetic chemistry.In chemical synthesis, Quinoline-4-carbonitrile acts as a key intermediate in the production of pharmaceuticals, agrochemicals, and materials. Its aromatic nature and cyano group make it a suitable candidate for the introduction of diverse functional groups through various chemical transformations. This compound is particularly useful in the synthesis of biologically active molecules, such as antimalarials, anti-inflammatory agents, and anticancer drugs.One common application of Quinoline-4-carbonitrile is its involvement in the synthesis of heterocyclic compounds, where it serves as a precursor for the construction of fused ring systems. Through efficient and selective chemical reactions, this compound can be modified to yield structurally intricate molecules with improved pharmacological properties and biological activities.Additionally, Quinoline-4-carbonitrile is utilized in the development of organic light-emitting diodes (OLEDs) and other advanced materials due to its electron-accepting properties and conjugated structure. By incorporating this compound into the chemical design of functional materials, researchers can tailor its properties to achieve specific electronic, optical, and physical characteristics.Overall, Quinoline-4-carbonitrile plays a significant role in chemical synthesis by enabling the efficient construction of complex organic molecules and functional materials with diverse applications in pharmaceuticals, agrochemicals, and advanced technologies.