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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-Pyridinemethanamine, 4-amino-

NCc1cnccc1N Request for Quotation
Chemical Name: 3-Pyridinemethanamine, 4-amino-
CAS Number: 158531-09-0
Product Number: AG001Q9M(AGN-PC-078TBV)
Synonyms:
MDL No:
Molecular Formula: C6H9N3
Molecular Weight: 123.1558

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Aminomethyl)pyridin-4-amine is a versatile compound widely used in chemical synthesis due to its unique reactivity and functional group properties. In organic chemistry, it serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials.One important application of 3-(Aminomethyl)pyridin-4-amine is in the formation of heterocyclic compounds. By utilizing its amino and pyridine moieties, chemists are able to efficiently construct complex ring structures with diverse functionalities. This compound is particularly valuable in the synthesis of nitrogen-containing heterocycles, which are prevalent in many biologically active molecules.Furthermore, 3-(Aminomethyl)pyridin-4-amine is utilized as a key intermediate in the preparation of ligands for coordination chemistry and organometallic complexes. Its amino functionality can serve as a chelating site for metal ions, enabling the formation of stable coordination complexes with various transition metals. These complexes find applications in catalysis, materials science, and medicinal chemistry.In addition to its role in heterocyclic synthesis and coordination chemistry, 3-(Aminomethyl)pyridin-4-amine is also employed in the development of novel biomolecules and molecular probes. Its unique structure offers opportunities for the design and synthesis of compounds with specific biological activities or targeting capabilities. Researchers leverage the reactivity of this compound to create bioactive molecules for drug discovery and chemical biology investigations.