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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-chlorophenyl)-

Clc1cccc(c1)N1CCOCC1 Request for Quotation
Chemical Name: Morpholine, 4-(3-chlorophenyl)-
CAS Number: 41605-90-7
Product Number: AG00CABI(AGN-PC-0NH2IT)
Synonyms:
MDL No:
Molecular Formula: C10H12ClNO
Molecular Weight: 197.6614

Identification/Properties

Properties
BP:
324°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
197.662g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
197.061g/mol
Monoisotopic Mass:
197.061g/mol
Topological Polar Surface Area:
12.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
159
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


4-(3-Chlorophenyl)morpholine, also known as $name$, serves as a versatile chemical reagent in various synthetic processes. Its unique molecular structure combines the functional groups of a chlorophenyl moiety with a morpholine ring, making it a valuable intermediate in pharmaceutical and agrochemical synthesis.In organic chemistry, $name$ can be utilized as a building block for the preparation of biologically active compounds, such as pharmaceutical drugs and crop protection agents. Its chlorophenyl group enables selective functionalization reactions, while the morpholine ring imparts favorable solubility and stability properties to the final products.Moreover, the presence of the morpholine moiety in $name$ can participate in diverse reactions, including nucleophilic substitution, reductive amination, and cyclization processes. This versatility allows for the synthesis of complex molecular structures in a controlled and efficient manner.Overall, the application of 4-(3-Chlorophenyl)morpholine in chemical synthesis offers researchers and chemists a valuable tool for designing and accessing novel compounds with potential applications in the fields of medicine, agriculture, and material science.