1-ethyl-2,3,3-trimethyl-3H-indol-1-ium-5-sulfonate

1-ethyl-2,3,3-trimethyl-3H-indol-1-ium-5-sulfonate

sodium (2S,3S,4S,5R,6S)-6-((5-bromo-4-chloro-1H-indol-3-yl)oxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylate

sodium (2S,3S,4S,5R,6S)-6-((5-bromo-4-chloro-1H-indol-3-yl)oxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylate

1-ethyl-2,3,3-trimethyl-3H-indol-1-ium iodide

$250.00
CAS No.: 14134-81-7
Catalog No.: 194543
Purity: 95%
MF: C13H18IN
MW: 315.198
Storage: 2-8 degree Celsius
SMILES: CC1(C)C(C)=[N+](CC)C2=C1C=CC=C2.[I-]
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1-ethyl-2,3,3-trimethyl-3H-indol-1-ium iodide; CAS No.: 14134-81-7; 1-ethyl-2,3,3-trimethyl-3H-indol-1-ium iodide. PROPERTIES: 1-ethyl-2,3,3-trimethyl-3H-indol-1-ium iodide is a crystalline solid. Its molecular formula is C12H15IN2, and the molecular weight is approximately 326.17 g/mol. The compound has a melting point of approximately 160-162 C. It is moderately soluble in water and commonly used in the form of its iodide salt. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a compound containing an indole ring, an ethyl group, three methyl groups, and an iodide counterion, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental ingestion, medical attention should be sought immediately. APPLICATIONS: In organic synthesis, 1-ethyl-2,3,3-trimethyl-3H-indol-1-ium iodide serves as a valuable intermediate. The indole ring provides opportunities for further functionalization. The iodide counterion can be involved in various reactions such as nucleophilic substitution. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain anticancer drugs, the structure of 1-ethyl-2,3,3-trimethyl-3H-indol-1-ium iodide can be modified to enhance the drug's ability to target cancer cells and improve its therapeutic index (as reported in medicinal chemistry journals). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as noted in organic chemistry research papers).

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