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Structure of 2408959-99-7
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This pyrrolopyridine-based amine features a dual protonation site, enhancing solubility and stability in aqueous media. The dihydrochloride salt form enables efficient handling and integration into synthetic workflows. This scaffold serves as a key building block for bioactive molecules in medicinal chemistry, particularly in kinase inhibitor development and CNS-targeted therapeutics.
(1H-Pyrrolo[3,2-c]pyridin-2-yl)methanamine dihydrochloride serves as a versatile building block for medicinal chemistry, enabling efficient access to pyrrolopyridine-based scaffolds. The amine functionality facilitates straightforward derivatization via reductive amination, coupling reactions, and salt formation, while the dihydrochloride form ensures excellent solubility and bench stability. Its compatibility with standard synthetic protocols makes it a practical choice for constructing bioactive heterocycles in drug discovery workflows.
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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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: