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Structure of 5054-94-4
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This indole derivative features a methanamine group at the 5-position of a 2,3-dimethyl-substituted indole core. The electron-rich aromatic system enhances reactivity in coupling processes, while the primary amine facilitates conjugation and functionalization. Designed for synthetic versatility, it serves as a key intermediate in bioactive molecule development.
(2,3-Dimethyl-1H-indol-5-yl)methanamine serves as a versatile building block for medicinal chemistry and materials science, enabling efficient access to substituted indole scaffolds. Its primary amine functionality facilitates straightforward derivatization via amidation, alkylation, and reductive amination, while the electron-rich indole core supports electrophilic substitution and transition-metal-catalyzed coupling reactions. The molecule exhibits good bench stability and is readily purified by chromatography or recrystallization, making it well-suited for scalable synthesis and high-throughput screening campaigns.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: