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Atomfair 1-Methyl-4-nitro-1H-indole C9H8N2O2 CAS 91482-63-2

1-Methyl-4-nitro-1H-indole (CAS No. 91482-63-2) is a high-purity nitro-substituted indole derivative with the molecular formula C9H8N2O2. This heterocyclic aromatic compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its versatile reactivity and structural features. The nitro group at the 4-position of the indole ring enhances its electrophilic properties, making it a valuable intermediate for further functionalization. Available in >98% purity (HPLC), this compound is rigorously tested for quality, ensuring optimal performance in synthetic applications. Suitable for researchers and industrial scientists, it is supplied in sealed packaging under inert conditions to maintain stability.

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Description

1-Methyl-4-nitro-1H-indole (CAS No. 91482-63-2) is a high-purity nitro-substituted indole derivative with the molecular formula C9H8N2O2. This heterocyclic aromatic compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its versatile reactivity and structural features. The nitro group at the 4-position of the indole ring enhances its electrophilic properties, making it a valuable intermediate for further functionalization. Available in >98% purity (HPLC), this compound is rigorously tested for quality, ensuring optimal performance in synthetic applications. Suitable for researchers and industrial scientists, it is supplied in sealed packaging under inert conditions to maintain stability.

Properties

  • CAS Number: 91482-63-2
  • Complexity: 214
  • IUPAC Name: 1-methyl-4-nitro-indole
  • InChI: InChI=1S/C9H8N2O2/c1-10-6-5-7-8(10)3-2-4-9(7)11(12)13/h2-6H,1H3
  • InChI Key: MGIRVUJGWSRAOV-UHFFFAOYSA-N
  • Exact Mass: 176.058577502
  • Molecular Formula: C9H8N2O2
  • Molecular Weight: 176.17
  • SMILES: CN1C=CC2=C1C=CC=C2[N+](=O)[O-]
  • Topological: 50.8
  • Monoisotopic Mass: 176.058577502
  • Synonyms: 1-methyl-4-nitro-1H-indole, 91482-63-2, DTXSID20524314, DTXCID60475119, 1-methyl-4-nitroindole, MFCD08236728, 1-methyl-4-nitro-1H-indol, SCHEMBL2475315, MGIRVUJGWSRAOV-UHFFFAOYSA-N, AKOS006284503, AB43866, AC-18590, AS-38397, SY242535, CS-0061754

Application

1-Methyl-4-nitro-1H-indole serves as a key building block in the synthesis of bioactive indole derivatives, including potential pharmaceuticals and agrochemicals. Its nitro group facilitates nucleophilic substitution reactions, enabling the development of novel heterocyclic compounds. Researchers also employ it in the study of indole-based fluorescent probes and optoelectronic materials. Additionally, it may be used as a precursor for catalytic transformations in medicinal chemistry.

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.

Disclaimer

Intended Use & Restrictions

This product is sold exclusively for laboratory research, analytical testing, or non-commercial purposes.

  • Strictly prohibited: Resale, repackaging, or formulation into commercial products.
  • Not approved for human/animal use, diagnostics, or manufacturing (including pharmaceuticals, agrochemicals, or consumer goods).

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