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Structure of 99071-54-2
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6-(Aminomethyl)quinoline features a strategically positioned aminomethyl group that enhances solubility and reactivity in synthetic transformations. This nitrogen-rich scaffold serves as a key building block in medicinal chemistry, enabling direct functionalization at the quinoline core. The pendant amine facilitates conjugation and metal coordination, supporting applications in catalyst design and bioconjugation.
6-(Aminomethyl)quinoline serves as a versatile building block in medicinal chemistry, enabling rapid access to biologically active scaffolds through straightforward functional group transformations. Its pendant primary amine facilitates conjugation, amidation, and reductive amination reactions, while the quinoline core provides a rigid, planar framework compatible with diverse heterocyclic extensions. The compound exhibits excellent bench stability and is readily purified by chromatography or recrystallization, making it ideal for high-throughput synthesis and lead optimization workflows.
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GHS Pictogram :
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GHS No : GHS07,GHS05
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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: