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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)-

Cyclopenta[c]pyrrol-4(2H)-one, 5,6-dihydro-

C1CC(=O)c2c1c[nH]c2 Request for Quotation
Chemical Name: Cyclopenta[c]pyrrol-4(2H)-one, 5,6-dihydro-
CAS Number: 95065-06-8
Product Number: AG005TFS(AGN-PC-07AF8A)
Synonyms:
MDL No:
Molecular Formula: C7H7NO
Molecular Weight: 121.1366

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
121.139g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
121.053g/mol
Monoisotopic Mass:
121.053g/mol
Topological Polar Surface Area:
32.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
144
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


5,6-Dihydrocyclopenta[c]pyrrol-4(2H)-one, a versatile compound utilized in chemical synthesis, serves as a valuable building block for the creation of various organic compounds. With its unique structure and reactivity, this molecule plays a crucial role in the development of complex chemical structures in the field of organic chemistry. It is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its cyclopentane ring and pyrrole core provide a solid foundation for the construction of more intricate molecular frameworks. Additionally, the presence of the carbonyl group offers opportunities for functionalization and diversification, allowing for the introduction of various chemical moieties to tailor the properties of the final products. In summary, the application of 5,6-Dihydrocyclopenta[c]pyrrol-4(2H)-one in chemical synthesis enables chemists to access a wide range of novel compounds with diverse functionalities and applications.