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Structure of 871826-15-2
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This bench-stable, moisture-tolerant amine features a chloropyridazinyl scaffold that integrates readily into medicinal chemistry scaffolds. The para-chloro substitution enhances electrophilic reactivity, enabling efficient coupling with nucleophiles under mild conditions. Its solubility profile supports use in diverse reaction media, streamlining synthesis workflows for heterocyclic compounds.
(6-Chloropyridazin-3-yl)methanamine serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling efficient construction of pyridazinyl-containing scaffolds. Its reactive chloro group facilitates nucleophilic substitution with amines, thiols, and other heteroatoms, while the pendant primary amine supports further functionalization via acylation, alkylation, or coupling reactions. The compound exhibits good bench stability and is readily purified by standard techniques, making it well-suited for scalable synthesis and API development workflows.
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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-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: