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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)-

5-(4-fluorophenyl)pyridine-2-carbonitrile

N#Cc1ccc(cn1)c1ccc(cc1)F Request for Quotation
Chemical Name: 5-(4-fluorophenyl)pyridine-2-carbonitrile
CAS Number: 914349-75-0
Product Number: AG00H02F(AGN-PC-07A1GY)
Synonyms:
MDL No:
Molecular Formula: C12H7FN2
Molecular Weight: 198.1958

Identification/Properties

Computed Properties
Molecular Weight:
198.2g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
198.059g/mol
Monoisotopic Mass:
198.059g/mol
Topological Polar Surface Area:
36.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
250
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:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(4-Fluorophenyl)picolinonitrile is a versatile chemical compound commonly used in chemical synthesis. This compound serves as a key building block in the preparation of various advanced materials and pharmaceutical intermediates. Its unique structure and reactivity make it a valuable tool for synthetic chemists seeking to create complex molecules with specific properties.One of the primary applications of 5-(4-Fluorophenyl)picolinonitrile is in the synthesis of heterocyclic compounds. By utilizing its aromatic fluorophenyl group and nitrile functionality, chemists can efficiently construct a wide range of heterocycles such as pyridines, pyrimidines, and quinolines. These heterocyclic compounds exhibit diverse biological activities and are essential components of many pharmaceuticals, agrochemicals, and materials.Furthermore, 5-(4-Fluorophenyl)picolinonitrile can be employed in transition metal-catalyzed cross-coupling reactions to form carbon-carbon bonds. This enables the incorporation of the fluorophenyl moiety into more elaborate molecular structures, enhancing the properties and functionalities of the final products. Such transformations are crucial in the development of new drugs, materials, and specialty chemicals.Overall, the strategic use of 5-(4-Fluorophenyl)picolinonitrile in chemical synthesis enables the efficient construction of complex molecules with tailored properties, making it a valuable tool for researchers in the fields of medicinal chemistry, materials science, and organic synthesis.