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Structure of 55556-57-5
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(1-Methyl-1H-indol-2-yl)methanamine features a methylated indole core with a primary amine tethered to the 1-position, delivering a polar, electron-rich scaffold. This configuration enhances solubility and reactivity in synthetic transformations, particularly in coupling reactions and bioconjugation workflows. The molecule exhibits bench-stable handling characteristics under standard conditions, enabling straightforward integration into medicinal chemistry and materials synthesis pipelines.
(1-Methyl-1H-indol-2-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling the synthesis of indole-based pharmaceuticals and bioactive heterocycles. The primary amine functionality facilitates straightforward derivatization via amidation, alkylation, and reductive amination, while the methyl-substituted indole core provides enhanced metabolic stability and favorable pharmacokinetic properties. Bench-stable and readily purified by column chromatography, it functions effectively in standard coupling protocols and supports scalable synthesis of targeted scaffolds.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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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-H318-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: