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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 that finds wide applications in chemical synthesis, particularly in the pharmaceutical industry. This unique molecule serves as an essential building block in the creation of various pharmaceutical agents, thanks to its structural properties and reactivity. With its ability to introduce specific functional groups and structural motifs, 2-Chloro-N-phenylisonicotinamide plays a crucial role in the development of novel drug molecules and therapeutic agents. Its presence often imparts desirable biological activities to the end products, making it a valuable tool in medicinal chemistry research. Additionally, the compound's compatibility with a range of synthetic methodologies enables chemists to efficiently access complex molecular structures, further expanding the scope of chemical synthesis possibilities in drug discovery and development.