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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, 3-(4-morpholinyl)-

Nc1cccc(c1)N1CCOCC1 Request for Quotation
Chemical Name: Benzenamine, 3-(4-morpholinyl)-
CAS Number: 159724-40-0
Product Number: AG001RCK(AGN-PC-0JWYM5)
Synonyms:
MDL No: MFCD03197165
Molecular Formula: C10H14N2O
Molecular Weight: 178.2310

Identification/Properties

Properties
MP:
118 °C
BP:
369.9°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
178.235g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
178.111g/mol
Monoisotopic Mass:
178.111g/mol
Topological Polar Surface Area:
38.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
157
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(4-Morpholinyl)aniline is a versatile compound commonly utilized in chemical synthesis for its unique structure and reactivity. In organic synthesis, this compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its morpholine moiety provides enhanced solubility and stability properties, making it ideal for use in the development of drug candidates and bioactive molecules. Additionally, the aniline group confers electron-donating and nucleophilic characteristics, facilitating its participation in a wide range of synthetic transformations such as nucleophilic aromatic substitution, palladium-catalyzed cross-coupling reactions, and reductive amination processes. The strategic incorporation of 3-(4-Morpholinyl)aniline into molecular structure enables fine-tuning of properties and functionalities, offering opportunities for the design and synthesis of novel compounds with diverse applications across the fields of medicinal chemistry, materials science, and chemical biology.