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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-(4-hydroxybenzoyl)-

O=C(c1ccc(cc1)O)N1CCOCC1 Request for Quotation
Chemical Name: Morpholine, 4-(4-hydroxybenzoyl)-
CAS Number: 18137-25-2
Product Number: AG0022UI(AGN-PC-0M1APN)
Synonyms:
MDL No:
Molecular Formula: C11H13NO3
Molecular Weight: 207.2258

Identification/Properties

Computed Properties
Molecular Weight:
207.229g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
207.09g/mol
Monoisotopic Mass:
207.09g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
218
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


The compound (4-Hydroxyphenyl)(morpholino)methanone, also known as $name$, is a versatile reagent commonly utilized in chemical synthesis processes. Its unique molecular structure allows for various applications in organic chemistry, particularly in the formation of complex structures and pharmaceutical intermediates.One of the key uses of (4-Hydroxyphenyl)(morpholino)methanone is as a building block in the synthesis of heterocyclic compounds. Its reactive functional groups enable selective modifications and efficient coupling reactions with other organic molecules, facilitating the creation of diverse chemical structures with specific functionalities.In addition, (4-Hydroxyphenyl)(morpholino)methanone serves as a valuable reagent in the development of novel pharmaceutical compounds. Its presence in drug synthesis can impart desirable biological activities or pharmacokinetic properties, making it an essential component in the production of potential therapeutic agents.Overall, the versatility and reactivity of (4-Hydroxyphenyl)(morpholino)methanone make it a valuable tool for synthetic chemists seeking to access complex molecular architectures and explore new avenues in chemical synthesis.