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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)-

1H-Pyrrole-2,5-dione, 1-(4-benzoylphenyl)-

O=C1C=CC(=O)N1c1ccc(cc1)C(=O)c1ccccc1 Request for Quotation
Chemical Name: 1H-Pyrrole-2,5-dione, 1-(4-benzoylphenyl)-
CAS Number: 92944-71-3
Product Number: AG003K8S(AGN-PC-0JMV2J)
Synonyms:
MDL No:
Molecular Formula: C17H11NO3
Molecular Weight: 277.27414

Identification/Properties

Properties
MP:
161-163ºC
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
277.279g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
277.074g/mol
Monoisotopic Mass:
277.074g/mol
Topological Polar Surface Area:
54.4A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
450
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Benzoylphenyl)-1H-pyrrole-2,5-dione, also known as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. In organic synthesis, $name$ serves as a valuable building block for the creation of various complex organic molecules. Its aromatic structure and electron-rich pyrrole ring make it an excellent candidate for the formation of diversified drug molecules, natural product derivatives, and functional materials. $name$ is commonly employed in the formation of heterocyclic compounds, which are essential in pharmaceutical and material science research. Additionally, its benzoyl group can undergo a range of transformations, such as reduction, oxidation, or substitution reactions, further expanding its synthetic utility in the development of novel chemical structures. The versatility and reactivity of 1-(4-Benzoylphenyl)-1H-pyrrole-2,5-dione make it an indispensable tool for chemists in the pursuit of innovative molecular design and synthesis strategies.