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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-Propenamide, N-(4-benzoylphenyl)-

C=CC(=O)Nc1ccc(cc1)C(=O)c1ccccc1 Request for Quotation
Chemical Name: 2-Propenamide, N-(4-benzoylphenyl)-
CAS Number: 22421-62-1
Product Number: AG003HWD(AGN-PC-000LTG)
Synonyms:
MDL No:
Molecular Formula: C16H13NO2
Molecular Weight: 251.2799

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
251.285g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
251.095g/mol
Monoisotopic Mass:
251.095g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
337
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


2-Propenamide, N-(4-benzoylphenyl)- is a key compound utilized in chemical synthesis for its diverse range of applications. This compound serves as a versatile building block in the production of various organic compounds due to its unique chemical structure and reactivity.Its primary use lies in the synthesis of pharmaceutical intermediates, where it acts as a crucial component in the creation of active pharmaceutical ingredients (APIs) for a wide array of medicinal products. Furthermore, 2-Propenamide, N-(4-benzoylphenyl)- finds applications in the development of specialty chemicals, such as agrochemicals, dyes, and polymers, due to its ability to undergo various chemical transformations.In addition, this compound plays a significant role in organic synthesis processes, including cross-coupling reactions, heterocycle formation, and peptide synthesis. Its incorporation in these reactions enables the efficient and selective formation of complex organic molecules with high purity and yield.Overall, 2-Propenamide, N-(4-benzoylphenyl)- is a crucial ingredient in chemical synthesis, contributing to the production of a wide range of valuable compounds across pharmaceuticals, specialty chemicals, and organic synthesis applications.