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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-[(2-methoxyphenyl)amino]-

COc1ccccc1Nc1ncccc1C(=O)O Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 2-[(2-methoxyphenyl)amino]-
CAS Number: 114501-02-9
Product Number: AG000ELT(AGN-PC-0KIOLW)
Synonyms:
MDL No:
Molecular Formula: C13H12N2O3
Molecular Weight: 244.2460

Identification/Properties

Computed Properties
Molecular Weight:
244.25g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
244.085g/mol
Monoisotopic Mass:
244.085g/mol
Topological Polar Surface Area:
71.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
285
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


The compound 2-((2-Methoxyphenyl)amino)nicotinic acid serves as a valuable building block in chemical synthesis, particularly in the area of pharmaceutical research and development. With its unique structure combining an amino group and a nicotinic acid moiety, this compound offers versatile reactivity and functionality that make it a key intermediate in the synthesis of various biologically active molecules. Its ability to undergo diverse chemical transformations, such as amidation, esterification, and cyclization, enables the efficient construction of complex molecular structures. Additionally, the presence of the nicotinic acid scaffold provides potential for modulating biological activity through interactions with specific receptors or enzymes. Overall, 2-((2-Methoxyphenyl)amino)nicotinic acid plays a crucial role in the strategic design and synthesis of novel compounds with potential pharmacological applications.