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Structure of 438571-18-7
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This pyrrolopyridine derivative features a reactive primary amine group appended to a fused heteroaromatic scaffold. The moiety integrates readily into molecular architectures requiring nitrogen-rich, electron-deficient platforms. Its bench-stable nature enables straightforward handling in synthetic workflows.
(1H-Pyrrolo[3,2-c]pyridin-2-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling direct incorporation of a rigid, electron-rich heterocyclic scaffold into target molecules. The primary amine functionality facilitates facile derivatization via amidation, alkylation, or reductive amination, while the pyrrolopyridine core exhibits favorable metabolic stability and π-stacking potential in kinase inhibitor design. Bench-stable and readily purified by standard chromatography, it functions effectively in solution-phase synthesis and supports scalable transformations.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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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: