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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-Pyridinecarboxamide, 2-chloro-N-phenyl-

Clc1nccc(c1)C(=O)Nc1ccccc1 Request for Quotation
Chemical Name: 4-Pyridinecarboxamide, 2-chloro-N-phenyl-
CAS Number: 80194-83-8
Product Number: AG003H2Z(AGN-PC-003NE6)
Synonyms:
MDL No: MFCD09817650
Molecular Formula: C12H9ClN2O
Molecular Weight: 232.6657

Identification/Properties

Properties
BP:
310.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
232.667g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
232.04g/mol
Monoisotopic Mass:
232.04g/mol
Topological Polar Surface Area:
42A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
241
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-N-phenylisonicotinamide is a versatile compound extensively used in chemical synthesis. Its unique structural properties make it an ideal building block for organic reactions, offering a wide range of applications in the field of medicinal chemistry, pharmaceuticals, and material science.2-Chloro-N-phenylisonicotinamide serves as a key intermediate in the synthesis of various biologically active compounds, including pharmaceutical agents and agrochemicals. It can undergo substitution reactions, cyclization, and condensation processes to generate diverse molecular architectures with tailored properties.In organic synthesis, 2-Chloro-N-phenylisonicotinamide acts as a valuable reagent for introducing the chloro functional group into target molecules, allowing chemists to modify the physicochemical properties of compounds. Its incorporation can enhance the bioactivity, stability, and solubility of final products, making it a crucial component in the development of novel drugs and materials.Furthermore, the presence of the phenyl and isonicotinamide moieties in this compound imparts additional reactivity and selectivity in synthetic transformations, enabling the construction of complex molecular frameworks efficiently. By harnessing the synthetic potential of 2-Chloro-N-phenylisonicotinamide, researchers can access a wide range of structurally diverse molecules with potential applications in various scientific fields.