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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, 4-[2-(4-morpholinyl)ethoxy]-

Nc1ccc(cc1)OCCN1CCOCC1 Request for Quotation
Chemical Name: Benzenamine, 4-[2-(4-morpholinyl)ethoxy]-
CAS Number: 52481-41-1
Product Number: AG00I9E5(AGN-PC-0LU5NR)
Synonyms:
MDL No:
Molecular Formula: C12H18N2O2
Molecular Weight: 222.2835

Identification/Properties

Computed Properties
Molecular Weight:
222.288g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
222.137g/mol
Monoisotopic Mass:
222.137g/mol
Topological Polar Surface Area:
47.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
188
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


4-(2-Morpholinoethoxy)aniline, also known as $name$, is a versatile compound widely used in chemical synthesis. This particular compound plays a crucial role as a building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure containing a morpholine ring and an aniline moiety contributes to its diverse applications in the synthesis of complex organic molecules.In chemical synthesis, 4-(2-Morpholinoethoxy)aniline serves as a key intermediate in the preparation of heterocyclic compounds and biologically active molecules. Its functional groups allow for various modifications and derivatizations, enabling synthetic chemists to tailor the molecule for specific applications. Moreover, the presence of both basic and aromatic functionalities in this compound makes it a valuable starting material for the creation of new compounds with enhanced properties.Additionally, 4-(2-Morpholinoethoxy)aniline exhibits good reactivity and compatibility with different reaction conditions, making it a popular choice in organic synthesis processes. Its ability to participate in coupling reactions, condensations, and other transformations make it a valuable tool for building complex molecular structures efficiently.Overall, the application of 4-(2-Morpholinoethoxy)aniline in chemical synthesis showcases its significance as a versatile intermediate for the creation of diverse compounds with potential therapeutic, agricultural, and industrial uses.