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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)-

Ethanone, 1-(4-nitro-1H-indol-3-yl)-

[O-][N+](=O)c1cccc2c1c(c[nH]2)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-(4-nitro-1H-indol-3-yl)-
CAS Number: 4769-95-3
Product Number: AG00D82A(AGN-PC-0NH9JH)
Synonyms:
MDL No:
Molecular Formula: C10H8N2O3
Molecular Weight: 204.1821

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Nitro-1H-indol-3-yl)ethanone is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. As a key building block in organic chemistry, this compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its ability to participate in diverse chemical reactions, including nucleophilic addition, acylation, and condensation, makes it a valuable tool for organic chemists. In particular, its nitro group can be selectively reduced to an amino group, enabling the functionalization of the molecule for further manipulation. Additionally, the presence of the indole ring confers aromaticity and stability, allowing for the creation of complex molecular scaffolds with diverse applications in drug discovery and material science.