3-alkylindoles
3-Alkylindoles are a class of heterocyclic compounds derived from indole, featuring an alkyl substituent at the 3-position. These molecules exhibit diverse applications due to their unique structural features and chemical properties. In the pharmaceutical industry, they are often explored for potential therapeutic effects such as anti-inflammatory, analgesic, and neuroprotective activities. Additionally, 3-alkylindoles have gained attention in the field of natural product chemistry, where they can be found in various plants and may contribute to their biological activities. Their aromatic nature also makes them valuable intermediates in organic synthesis, offering opportunities for functional group modifications and derivatization. The diverse range of alkyl substituents allows for fine-tuning of properties and can influence the compounds' solubility, stability, and reactivity, making 3-alkylindoles a versatile class of molecules with significant potential in both research and commercial applications.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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1H-Indole, 3-(4-pyridinylmethyl)- | 5275-07-0 | C14H12N2 |
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1H-Indole, 6-methoxy-3-(4-piperidinyl)- | 52157-78-5 | C14H18N2O |
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4-(5-Bromo-1H-indol-3-yl)-2-butanone | 552314-85-9 | C12H12BrNO |
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1H-Indole, 7-methoxy-2,3-dimethyl- | 53918-89-1 | C11H13NO |
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1H-Indole, 5-bromo-3-ethyl-2-methyl- | 646038-04-2 | C11H12BrN |
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Ethyl 8-Fluoro-1,3,4,5-Tetrahydro-2h-Pyrido4,3-BIndole-2-Carboxylate | 58038-66-7 | C14H15FN2O2 |
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4-Thiazolecarboxamide,2-[(1S)-1-aminoethyl]-N-[2-(1H-indol-3-yl)ethyl]- | 58887-22-2 | C16H18N4OS |
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4,6-dimethoxy-3-methyl-1H-Indole | 74973-30-1 | C11H13NO2 |
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7-Methyltryptophol | 39232-85-4 | C11H13NO |
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5-Methoxy-3-methyl-1H-indole-2-carbaldehyde | 30464-90-5 | C11H11NO2 |
Related Literature
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Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
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Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
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Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
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