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Structure of 2521-13-3
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5-Methoxy-1-methyl-1H-indole is a substituted indole featuring a methoxy group at the 5-position and a methyl substituent at the nitrogen. This electron-rich scaffold offers enhanced stability and solubility in organic media, enabling efficient incorporation into bioactive molecules. The para-methoxy substitution modulates electronic properties for use in medicinal chemistry and fluorescent probe development.
5-Methoxy-1-methyl-1H-indole serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to substituted indole scaffolds. Its methoxy and methyl substituents provide favorable electronic modulation and enhanced stability, facilitating downstream functionalization via electrophilic substitution or transition-metal-catalyzed coupling. The compound exhibits excellent bench stability and compatibility with common purification methods, making it well-suited for scalable synthesis of bioactive molecules.
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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 : P260-P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: