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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-cyanobenzoyl)-

N#Cc1ccc(cc1)C(=O)N1CCOCC1 Request for Quotation
Chemical Name: Morpholine, 4-(4-cyanobenzoyl)-
CAS Number: 87294-97-1
Product Number: AG004LR5(AGN-PC-00SGXI)
Synonyms:
MDL No:
Molecular Formula: C12H12N2O2
Molecular Weight: 216.2359

Identification/Properties

Computed Properties
Molecular Weight:
216.24g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
216.09g/mol
Monoisotopic Mass:
216.09g/mol
Topological Polar Surface Area:
53.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
293
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-(Morpholine-4-carbonyl)benzonitrile, also known as $name$, is a versatile compound commonly utilized in chemical synthesis. This compound plays a crucial role in the development of pharmaceuticals and agrochemicals. Its unique structure combines the functionality of both a nitrile group and a morpholine ring, making it a valuable building block in organic chemistry.In chemical synthesis, 4-(Morpholine-4-carbonyl)benzonitrile is frequently employed as a key intermediate for the creation of various bioactive molecules. Its morpholine moiety offers a high degree of steric hindrance, making it a suitable candidate for reactions involving sensitive substrates. Additionally, the nitrile group provides a versatile handle for further modifications, enabling the synthesis of diverse compounds with tailored properties.One notable application of 4-(Morpholine-4-carbonyl)benzonitrile is its use in the synthesis of potential drug candidates. By incorporating this compound into synthetic routes, chemists can access novel derivatives with enhanced biological activities. Furthermore, its presence in the molecular structure can impart desirable pharmacokinetic properties, making it a valuable component in drug discovery efforts.Moreover, 4-(Morpholine-4-carbonyl)benzonitrile serves as a valuable building block in the development of agrochemicals. Its structural features can be leveraged to introduce specific functionalities that enhance the efficacy and selectivity of pesticides and herbicides. Through strategic synthetic manipulations, chemists can generate targeted molecules that exhibit improved agronomic performance and reduced environmental impact.Overall, the application of 4-(Morpholine-4-carbonyl)benzonitrile in chemical synthesis underscores its significance as a versatile intermediate in the creation of biologically active compounds and agrochemicals. Its unique structural characteristics and functional diversity make it a valuable asset in the pursuit of innovative molecules with potential applications in pharmaceuticals and agriculture.