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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, 3-methyl-6-nitro-

[O-][N+](=O)c1ccc2c(c1)[nH]cc2C Request for Quotation
Chemical Name: 1H-Indole, 3-methyl-6-nitro-
CAS Number: 133053-76-6
Product Number: AG0011L7(AGN-PC-0KT1BD)
Synonyms:
MDL No:
Molecular Formula: C9H8N2O2
Molecular Weight: 176.1720

Identification/Properties

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


3-Methyl-6-nitro-1H-indole is a valuable chemical compound frequently utilized in chemical synthesis for a variety of applications. Its unique structure and properties make it a versatile building block in the creation of various organic compounds. In chemical synthesis, 3-Methyl-6-nitro-1H-indole serves as a key intermediate for the production of pharmaceuticals, agrochemicals, and dyes. Its functional groups, including the nitro group and the indole ring system, enable it to participate in diverse reactions such as nucleophilic substitution, reduction, and condensation processes. One of the notable applications of 3-Methyl-6-nitro-1H-indole is in the synthesis of indole-based drugs and biologically active molecules. By modifying the functional groups attached to the indole ring, chemists can tailor the compound's properties to develop new pharmaceuticals with enhanced biological activities or improved pharmacokinetic profiles.Furthermore, 3-Methyl-6-nitro-1H-indole is also used as a precursor in the synthesis of indole dyes, which find applications in the textile industry for coloring fabrics. The presence of the nitro group in the molecule allows for the introduction of various colorants through chemical reactions, resulting in a wide range of vibrant dye molecules.Overall, the versatile nature of 3-Methyl-6-nitro-1H-indole makes it an essential component in the toolkit of synthetic chemists for the creation of diverse organic compounds with applications across various industries.