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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)-

2-(pyridin-4-ylmethylamino)pyridine-3-carboxylic acid

OC(=O)c1cccnc1NCc1ccncc1 Request for Quotation
Chemical Name: 2-(pyridin-4-ylmethylamino)pyridine-3-carboxylic acid
CAS Number: 854382-06-2
Product Number: AG004JXS(AGN-PC-05G4AJ)
Synonyms:
MDL No:
Molecular Formula: C12H11N3O2
Molecular Weight: 229.2346

Identification/Properties

Properties
BP:
461.7±40.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
229.239g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
229.085g/mol
Monoisotopic Mass:
229.085g/mol
Topological Polar Surface Area:
75.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
254
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-((Pyridin-4-ylmethyl)amino)nicotinic acid, also known as $name$, is a versatile compound that finds extensive application in chemical synthesis. Its unique structure, incorporating both a pyridine ring and a nicotinic acid moiety, allows it to participate in various synthetic pathways, leading to the formation of diverse organic compounds. In chemical synthesis, $name$ can serve as a key building block for the preparation of pharmaceutical intermediates, agrochemicals, and functional materials. Its amino group can undergo selective functionalization reactions, enabling the introduction of different substituents for fine-tuning the properties of the final product. The presence of the nicotinic acid group provides additional reactivity, allowing for the formation of heterocyclic structures with enhanced biological activity.Moreover, the pyridine ring in $name$ can participate in cross-coupling reactions, such as Suzuki-Miyaura and Heck coupling, to generate complex molecular architectures efficiently. This compound's versatility and reactivity make it a valuable tool for organic chemists seeking to access novel compounds for various applications in the fields of medicinal chemistry, materials science, and beyond.