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Structure of 5192-23-4
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4-Aminoindole features a strategically positioned amino group that enhances electron density at the indole core, enabling efficient incorporation into conjugated systems. This functionalization supports direct coupling in heterocyclic synthesis and facilitates access to bioactive scaffolds under standard conditions.
4-Aminoindole serves as a versatile building block in medicinal chemistry, enabling direct incorporation into heterocyclic scaffolds via standard coupling reactions. Its ortho-amino functionality facilitates electrophilic substitution and transition-metal-catalyzed transformations, while the indole core provides inherent stability and π-conjugation. The compound exhibits favorable bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthesis workflows in API development.
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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 : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: