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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)-

2-(2-methoxyphenyl)morpholine

COc1ccccc1C1CNCCO1 Request for Quotation
Chemical Name: 2-(2-methoxyphenyl)morpholine
CAS Number: 1001940-35-7
Product Number: AG000176(AGN-PC-04FWSC)
Synonyms:
MDL No:
Molecular Formula: C11H15NO2
Molecular Weight: 193.2423

Identification/Properties

Computed Properties
Molecular Weight:
193.246g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
193.11g/mol
Monoisotopic Mass:
193.11g/mol
Topological Polar Surface Area:
30.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
175
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


2-(2-Methoxyphenyl)morpholine, also known as morpholine-2-(2-methoxyphenyl), is a versatile chemical compound widely employed in organic synthesis. This compound plays a crucial role in the field of chemical synthesis due to its unique structure and reactivity.One of the primary applications of 2-(2-Methoxyphenyl)morpholine in chemical synthesis is as a building block for the preparation of various pharmaceutical compounds. Its morpholine ring provides a stable and versatile scaffold for the attachment of different functional groups, allowing for the synthesis of diverse drug molecules. Additionally, the presence of the 2-methoxyphenyl group imparts specific properties and reactivity to the compound, further expanding its utility in drug development.Furthermore, 2-(2-Methoxyphenyl)morpholine is often utilized as a nucleophilic catalyst in various organic transformations. Its ability to participate in nucleophilic substitution reactions makes it a valuable tool in the synthesis of complex organic molecules. By acting as a nucleophile, this compound can facilitate the formation of new carbon-carbon and carbon-heteroatom bonds, enabling the construction of intricate molecular structures.Overall, the application of 2-(2-Methoxyphenyl)morpholine in chemical synthesis extends to the synthesis of pharmaceuticals and other organic compounds, highlighting its importance as a key building block in the field of organic chemistry.