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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-(PYRIDIN-2-YL)PHENYL]METHANAMINE

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Chemical Name: [3-(PYRIDIN-2-YL)PHENYL]METHANAMINE
CAS Number: 859915-26-7
Product Number: AG00IDUF(AGN-PC-0WAKY4)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
184.242g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
184.1g/mol
Monoisotopic Mass:
184.1g/mol
Topological Polar Surface Area:
38.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
170
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 versatile compound (3-(Pyridin-2-yl)phenyl)methanamine, commonly known as $name$, plays a vital role in chemical synthesis as an important building block for various organic reactions. This compound is frequently utilized in the pharmaceutical and agrochemical industries for the synthesis of diverse molecules with biological activity. It serves as a key intermediate in the creation of heterocyclic compounds, which are essential in drug discovery and development processes. Additionally, $name$ is employed in the preparation of functional materials and specialty chemicals due to its unique structural properties. Its flexibility in forming bonds and its reactivity make it a valuable asset in the hands of synthetic chemists striving to create innovative compounds for a wide range of applications.