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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-Pyridinemethanamine, N-phenyl-

c1ccc(cc1)NCc1ccccn1 Request for Quotation
Chemical Name: 2-Pyridinemethanamine, N-phenyl-
CAS Number: 4329-81-1
Product Number: AG00I8BB(AGN-PC-0JLR3A)
Synonyms:
MDL No:
Molecular Formula: C12H12N2
Molecular Weight: 184.2371

Identification/Properties

Computed Properties
Molecular Weight:
184.242g/mol
XLogP3:
2.4
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:
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(Pyridin-2-ylmethyl)aniline, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties. This compound serves as a valuable building block in the assembly of organic molecules, particularly in the pharmaceutical and agrochemical industries. With its pyridine ring and aniline moiety, $name$ acts as a crucial intermediate in the creation of various biologically active compounds and specialty chemicals. It plays a vital role in the development of new drugs, pesticides, and other fine chemicals through its involvement in multi-step synthesis strategies. Additionally, the presence of the pyridine group in $name$ imparts specific reactivity and functionality that enable the formation of diverse molecular structures with tailored properties. In organic synthesis, N-(Pyridin-2-ylmethyl)aniline is a key component that facilitates the construction of complex molecules with precise control over stereochemistry and functional group positioning. This compound's significance lies in its ability to enable the synthesis of novel compounds with potential applications across various industries, highlighting its importance in advancing the field of chemical science.