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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-Pyridinecarboxylic acid, 2-(phenylamino)-

OC(=O)c1cccnc1Nc1ccccc1 Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 2-(phenylamino)-
CAS Number: 16344-24-4
Product Number: AG001U4N(AGN-PC-0K5UAI)
Synonyms:
MDL No:
Molecular Formula: C12H10N2O2
Molecular Weight: 214.2200

Identification/Properties

Computed Properties
Molecular Weight:
214.224g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
214.074g/mol
Monoisotopic Mass:
214.074g/mol
Topological Polar Surface Area:
62.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
239
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Phenylamino)nicotinic acid, also known as nicotinic acid phenylamide, serves as a versatile building block in organic synthesis due to its unique chemical properties. This compound is widely utilized in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its aromatic phenyl group provides a reactive site for coupling reactions, allowing for the formation of complex molecular structures. Additionally, the carboxylic acid functionality enables it to participate in esterification, amidation, and other important synthetic transformations. By incorporating 2-(Phenylamino)nicotinic acid into the synthesis of target compounds, chemists can efficiently access novel molecules with diverse biological activities and potential industrial applications.