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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)-

Benzenamine, 2-(3-pyridinyloxy)-

Nc1ccccc1Oc1cccnc1 Request for Quotation
Chemical Name: Benzenamine, 2-(3-pyridinyloxy)-
CAS Number: 76167-49-2
Product Number: AG0057N1(AGN-PC-0NJUCR)
Synonyms:
MDL No:
Molecular Formula: C11H10N2O
Molecular Weight: 186.2099

Identification/Properties

Computed Properties
Molecular Weight:
186.214g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
186.079g/mol
Monoisotopic Mass:
186.079g/mol
Topological Polar Surface Area:
48.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
175
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:
H302-H317
Precautionary Statements:
P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Pyridin-3-yloxy)aniline is a versatile compound widely utilized in chemical synthesis, specifically in the realm of organic chemistry. This compound serves as a key building block for the construction of various heterocyclic molecules and complex organic structures. It possesses unique structural features that make it a valuable tool in the development of novel pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-(Pyridin-3-yloxy)aniline is often employed as a coupling partner in transition metal-catalyzed cross-coupling reactions. This allows for the efficient formation of C-N bonds, enabling the creation of diverse organic compounds. Additionally, its pyridine moiety can participate in various functional group transformations, further expanding its synthetic utility.Furthermore, owing to its aromatic nature and electron-rich aniline group, 2-(Pyridin-3-yloxy)aniline can participate in aromatic substitution reactions, enabling the introduction of additional functional groups at specific positions on the molecule. This versatility makes it a valuable tool for the elaboration of molecular complexity in organic synthesis.Overall, the application of 2-(Pyridin-3-yloxy)aniline in chemical synthesis enables chemists to access a wide array of structurally diverse compounds with potential applications across multiple industries.