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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-Pyridinamine, N-(phenylmethyl)-

c1ccc(cc1)CNc1ccncc1 Request for Quotation
Chemical Name: 4-Pyridinamine, N-(phenylmethyl)-
CAS Number: 13556-71-3
Product Number: AG009AYW(AGN-PC-0O185O)
Synonyms:
MDL No:
Molecular Formula: C12H12N2
Molecular Weight: 184.2371

Identification/Properties

Computed Properties
Molecular Weight:
184.242g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
184.1g/mol
Monoisotopic Mass:
184.1g/mol
Topological Polar Surface Area:
24.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
146
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


N-Benzylpyridin-4-amine, also known as $name$, is a versatile intermediate compound widely used in chemical synthesis processes. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural properties and reactivity.In chemical synthesis, $name$ plays a crucial role as a starting material for the production of complex molecules. Its benzyl and pyridine moieties provide a valuable platform for the introduction of different functional groups through various synthetic manipulations such as acylation, alkylation, and halogenation.Moreover, the presence of the amine group in N-Benzylpyridin-4-amine grants it the ability to participate in important reactions like reductive amination, nucleophilic substitution, and metal-catalyzed cross-coupling. This enables chemists to efficiently create a diverse array of compounds with tailored properties and functionalities.Overall, the versatile application of N-Benzylpyridin-4-amine in chemical synthesis makes it a valuable tool for generating new molecules with potential applications in pharmaceuticals, materials science, and other chemical industries.