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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-Pyridinamine, N-(2-furanylmethyl)-

c1ccc(nc1)NCc1ccco1 Request for Quotation
Chemical Name: 2-Pyridinamine, N-(2-furanylmethyl)-
CAS Number: 46230-01-7
Product Number: AG00DWBD(AGN-PC-0JNQZ2)
Synonyms:
MDL No: MFCD00272277
Molecular Formula: C10H10N2O
Molecular Weight: 174.1992

Identification/Properties

Computed Properties
Molecular Weight:
174.203g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
174.079g/mol
Monoisotopic Mass:
174.079g/mol
Topological Polar Surface Area:
38.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
152
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


The application of N-(furan-2-ylmethyl)pyridin-2-amine in chemical synthesis is notable in the field of organic chemistry. This compound serves as a versatile building block for the construction of complex molecules due to its functional groups and reactivity. In synthetic chemistry, N-(furan-2-ylmethyl)pyridin-2-amine can participate in various reactions such as cross-coupling, nucleophilic addition, and cyclization reactions.The furan moiety in the molecule offers a site for potential electrophilic aromatic substitution reactions, enabling the introduction of diverse substituents to tailor the properties of the final product. Additionally, the pyridine ring confers aromaticity and can act as a directing group in transition metal-catalyzed reactions, facilitating the selective functionalization of specific positions within the molecule.Moreover, the amine functional group can serve as a nucleophile in various reactions, adding further versatility to the molecule's synthetic utility. Overall, the strategic placement of these functional groups in N-(furan-2-ylmethyl)pyridin-2-amine makes it a valuable intermediate for the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties.