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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-Quinolinecarbonitrile

N#Cc1cnc2c(c1)cccc2 Request for Quotation
Chemical Name: 3-Quinolinecarbonitrile
CAS Number: 34846-64-5
Product Number: AG003JWG(AGN-PC-0JM001)
Synonyms:
MDL No:
Molecular Formula: C10H6N2
Molecular Weight: 154.1680

Identification/Properties

Properties
MP:
108-110 °C
BP:
323.7°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
154.172g/mol
XLogP3:
1.6
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+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Cyanoquinoline is a versatile compound that finds wide utility in chemical synthesis. Its unique structure and reactivity make it a valuable building block for various organic transformations. In organic synthesis, 3-Cyanoquinoline serves as a key intermediate for the preparation of numerous biologically active molecules, pharmaceuticals, agrochemicals, and materials. Its presence in these molecular structures imparts significant biological and pharmacological properties, making it an essential component in drug discovery and development processes. Furthermore, 3-Cyanoquinoline is utilized in the synthesis of heterocyclic compounds and as a ligand in coordination chemistry, exhibiting diverse coordination modes to metal ions. Its ability to participate in various reactions such as nucleophilic substitution, condensation, and cycloaddition reactions expands its synthetic potential for the construction of complex molecular architectures. Along with its synthetic applications, 3-Cyanoquinoline also serves as a valuable probe in chemical biology and medicinal chemistry research, aiding in the understanding of biological processes and disease mechanisms. Its versatility and broad utility make 3-Cyanoquinoline a crucial component in modern chemical synthesis strategies.