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Structure of 1484-19-1
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3-Ethyl-1H-indole features a sterically accessible indole core with enhanced solubility and stability compared to unsubstituted analogs. This derivative integrates readily into bioactive scaffolds, enabling efficient access to functionalized heterocycles in medicinal chemistry and materials science applications.
3-Ethyl-1H-indole serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, offering a stable, bench-ready scaffold for C3 functionalization. Its electron-rich indole core facilitates electrophilic substitution and transition-metal-catalyzed coupling reactions, while the alkyl substituent enhances solubility and metabolic stability. Functions effectively in the construction of bioactive molecules and pharmaceutical intermediates.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: