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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-Indole, 4,6-dinitro-

[O-][N+](=O)c1cc2[nH]ccc2c(c1)[N+](=O)[O-] Request for Quotation
Chemical Name: 1H-Indole, 4,6-dinitro-
CAS Number: 245524-93-0
Product Number: AG002OIS(AGN-PC-0LE9YU)
Synonyms:
MDL No:
Molecular Formula: C8H5N3O4
Molecular Weight: 207.1430

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Chemical Structure


1H-Indole, 4,6-dinitro- is a versatile compound widely utilized in chemical synthesis due to its unique reactivity and structural properties. Commonly known for its electron-withdrawing nitro groups at the 4 and 6 positions, this compound serves as a valuable building block in the preparation of various complex organic molecules.In organic synthesis, 1H-Indole, 4,6-dinitro- is often employed as a key intermediate in the construction of biologically active compounds, pharmaceuticals, and agrochemicals. The presence of the dinitro groups imparts regioselectivity and can participate in various substitution reactions, enabling the creation of diverse chemical structures.Furthermore, the molecule's aromatic nature and nitrogen-containing heterocyclic backbone make it a pivotal component in the design and synthesis of heterocyclic compounds with potential applications in medicinal chemistry and material science. By harnessing the reactivity of 1H-Indole, 4,6-dinitro-, chemists can access a broad array of functionalized derivatives with tailored properties for specific applications in the field of organic chemistry.