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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, 3,4-di-1H-indol-3-yl-1-methyl-

O=C1N(C)C(=O)C(=C1c1c[nH]c2c1cccc2)c1c[nH]c2c1cccc2 Request for Quotation
Chemical Name: 1H-Pyrrole-2,5-dione, 3,4-di-1H-indol-3-yl-1-methyl-
CAS Number: 113963-68-1
Product Number: AG000A5M(AGN-PC-0JK689)
Synonyms:
MDL No:
Molecular Formula: C21H15N3O2
Molecular Weight: 341.3627

Identification/Properties

Computed Properties
Molecular Weight:
341.37g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
341.116g/mol
Monoisotopic Mass:
341.116g/mol
Topological Polar Surface Area:
69A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
604
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#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3,4-Di(1H-indol-3-yl)-1-methyl-1H-pyrrole-2,5-dione is a versatile building block in chemical synthesis due to its unique structure and reactivity. It features two indole groups and a pyrrole-dione core, making it a valuable intermediate for the construction of complex organic molecules. In chemical synthesis, 3,4-Di(1H-indol-3-yl)-1-methyl-1H-pyrrole-2,5-dione can serve as a key component for the generation of heterocyclic compounds with potential pharmaceutical applications. Its presence allows for the introduction of indole and pyrrole moieties into target molecules, enhancing their biological activity and specificity.Furthermore, the compound's structural features make it highly adaptable for the formation of fused ring systems and functional group manipulation. This enables chemists to explore various synthetic pathways for the development of new drug candidates, agrochemicals, and materials with tailored properties.Overall, the strategic incorporation of 3,4-Di(1H-indol-3-yl)-1-methyl-1H-pyrrole-2,5-dione in chemical synthesis offers a robust platform for the creation of diverse molecular architectures and the advancement of cutting-edge research in organic chemistry.