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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)-

Benzenemethanamine, N-methyl-3-phenoxy-

CNCc1cccc(c1)Oc1ccccc1 Request for Quotation
Chemical Name: Benzenemethanamine, N-methyl-3-phenoxy-
CAS Number: 129535-78-0
Product Number: AG000Z76(AGN-PC-0N5Q1H)
Synonyms:
MDL No: MFCD02089413
Molecular Formula: C14H15NO
Molecular Weight: 213.2750

Identification/Properties

Properties
BP:
313.868 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
213.28g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
213.115g/mol
Monoisotopic Mass:
213.115g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
189
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-Methyl-1-(3-phenoxyphenyl)methanamine is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound is commonly employed as a key building block in the development of various pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, N-Methyl-1-(3-phenoxyphenyl)methanamine serves as a valuable precursor in the preparation of structurally diverse molecules through functional group transformations. Its amine functionality allows for a wide range of synthetic manipulations, such as nucleophilic substitutions, condensation reactions, and metal-catalyzed transformations.Moreover, the presence of the phenoxyphenyl moiety in N-Methyl-1-(3-phenoxyphenyl)methanamine imparts specific steric and electronic properties that are crucial for influencing the physicochemical characteristics and biological activities of the synthesized compounds. This structural motif can participate in aromatic substitution reactions, oxidative coupling processes, and heterocyclic formation, enabling the creation of novel chemical entities with tailored properties.Overall, the application of N-Methyl-1-(3-phenoxyphenyl)methanamine in chemical synthesis offers researchers and chemists a powerful tool for designing and accessing a wide array of molecular structures with potential applications in various fields of science and technology.