Description
4-Fluoro-6-methyl-1H-indole (CAS No. 885522-13-4) is a high-purity fluorinated indole derivative with the molecular formula C9H8FN. This compound is a valuable building block in organic synthesis and pharmaceutical research, offering unique reactivity due to the presence of both fluorine and methyl substituents on the indole scaffold. Its well-defined structure (IUPAC name: 4-fluoro-6-methyl-1H-indole) ensures consistent performance in synthetic applications. The product is rigorously tested for purity and stability, making it ideal for demanding research environments. Available in various quantities, it is supplied with comprehensive analytical data (including NMR and HPLC) to meet the stringent requirements of medicinal chemists and material scientists.
Properties
- CAS Number: 885522-13-4
- Complexity: 148
- IUPAC Name: 4-fluoro-6-methyl-1H-indole
- InChI: InChI=1S/C9H8FN/c1-6-4-8(10)7-2-3-11-9(7)5-6/h2-5,11H,1H3
- InChI Key: NKHBDLUXWLINSD-UHFFFAOYSA-N
- Exact Mass: 149.064077422
- Molecular Formula: C9H8FN
- Molecular Weight: 149.16
- SMILES: CC1=CC2=C(C=CN2)C(=C1)F
- Topological: 15.8
- Monoisotopic Mass: 149.064077422
- Synonyms: 4-Fluoro-6-methyl-1H-indole, 885522-13-4, 4-Fluoro-6-methyl indole, SCHEMBL15895157, DTXSID80646501, AKOS006287796, AS-58984, DB-184860, CS-0326095, E83743
Application
4-Fluoro-6-methyl-1H-indole serves as a key intermediate in the synthesis of pharmacologically active compounds, particularly in the development of fluorinated drug candidates. Its structural features make it suitable for Suzuki-Miyaura coupling and other cross-coupling reactions to create diverse indole-based scaffolds. Researchers also utilize this compound in the study of enzyme inhibition and receptor binding due to its electron-withdrawing fluorine moiety.
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