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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)-

Morpholine, 4-(3-aminobenzoyl)-

Nc1cccc(c1)C(=O)N1CCOCC1 Request for Quotation
Chemical Name: Morpholine, 4-(3-aminobenzoyl)-
CAS Number: 104775-65-7
Product Number: AG007GKR(AGN-PC-0LU5XG)
Synonyms:
MDL No:
Molecular Formula: C11H14N2O2
Molecular Weight: 206.2411

Identification/Properties

Computed Properties
Molecular Weight:
206.245g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
206.106g/mol
Monoisotopic Mass:
206.106g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
227
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


As a versatile chemical intermediate, (3-Aminophenyl)(morpholino)methanone serves a crucial role in chemical synthesis. It exhibits exceptional reactivity and selectivity, making it a valuable building block in the creation of various pharmaceuticals, fine chemicals, and advanced materials.By harnessing the unique properties of (3-Aminophenyl)(morpholino)methanone, chemists can efficiently introduce functional groups, such as amines and ketones, into target molecules. This compound's ability to undergo diverse chemical transformations, including acylation, reduction, and condensation reactions, makes it an indispensable tool for creating complex organic structures.Furthermore, (3-Aminophenyl)(morpholino)methanone plays a key role in the synthesis of bioactive compounds and drug candidates. Its incorporation in medicinal chemistry projects enables the development of novel pharmaceuticals with enhanced therapeutic properties and reduced side effects. Additionally, it facilitates the construction of molecular scaffolds with specific pharmacological activities, paving the way for the discovery of new treatments for various diseases.In the realm of materials science, the incorporation of (3-Aminophenyl)(morpholino)methanone enables the synthesis of functional polymers, dyes, and catalysts with tailored properties. Its compatibility with different chemical reactions and its ability to modulate material characteristics make it a valuable tool for designing advanced materials with desired properties, such as conductivity, optical activity, and catalytic efficiency.Overall, the application of (3-Aminophenyl)(morpholino)methanone in chemical synthesis showcases its immense potential in driving innovation across diverse scientific fields. Its versatility, reactivity, and compatibility with various synthetic methodologies make it a valuable asset for researchers seeking to develop novel compounds and materials with tailored functionalities and applications.