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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, 1-methyl-6-nitro-

[O-][N+](=O)c1ccc2c(c1)n(C)cc2 Request for Quotation
Chemical Name: 1H-Indole, 1-methyl-6-nitro-
CAS Number: 99459-48-0
Product Number: AG0065GU(AGN-PC-0N7FQF)
Synonyms:
MDL No:
Molecular Formula: C9H8N2O2
Molecular Weight: 176.1720

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
176.175g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
176.059g/mol
Monoisotopic Mass:
176.059g/mol
Topological Polar Surface Area:
50.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
214
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#:
-
Hazard Statements:
H302-H317
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methyl-6-nitro-1H-indole, also known as $name$, is a versatile compound widely used in chemical synthesis. Due to its unique structure and properties, it serves as a key building block in the production of various organic compounds. In the realm of drug discovery and development, this compound is employed as a crucial intermediate in the synthesis of pharmaceutical agents and bioactive molecules.In organic synthesis, 1-Methyl-6-nitro-1H-indole plays a pivotal role as a precursor in the construction of complex organic molecules. Its ability to undergo diverse chemical transformations makes it a valuable tool for the creation of new materials, functionalized derivatives, and intricate molecular structures. Additionally, this compound exhibits reactivity patterns that enable the selective modification of specific functional groups, facilitating the tailoring of molecular properties to suit desired applications.Furthermore, the incorporation of 1-Methyl-6-nitro-1H-indole in chemical reactions allows for the synthesis of compounds with diverse pharmacological activities, making it an essential component in the development of novel therapeutic agents. Its presence in the synthetic route of pharmaceutical intermediates enhances the efficiency and selectivity of the overall process, leading to the creation of potential drug candidates with improved biological activity and reduced side effects.Overall, the utilization of 1-Methyl-6-nitro-1H-indole in chemical synthesis offers a wide range of applications in the organic chemistry field, showcasing its significance in the creation of valuable compounds with pharmaceutical, agrochemical, and material science applications.