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Structure of 4837-90-5
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4-Methoxyindole was used for comparing the complexation reaction of -cyclodextrin (-CD) with pindolol using reversed-phase liquid chromatography.
4-Methoxyindole serves as a versatile building block in medicinal chemistry and natural product synthesis, offering enhanced solubility and electronic modulation over unsubstituted indole. Its methoxy group enables selective functionalization at the 5- or 6-position via electrophilic substitution, while maintaining stability under standard coupling conditions. The molecule functions effectively in Pd-catalyzed cross-coupling reactions and serves as a key scaffold in heterocyclic drug discovery programs requiring balanced lipophilicity and metabolic stability.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: