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Structure of 18232-91-2
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2-Chloro-5-methylpyridine-3,4-diamine features a pyridine core with strategically positioned chloro and methyl groups, enabling selective functionalization. The diamine moiety provides dual amine handles for coupling reactions, while the electron-deficient ring enhances reactivity in nucleophilic substitution processes. This compound serves as a key intermediate in pharmaceutical synthesis.
2-Chloro-5-methylpyridine-3,4-diamine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based heterocycles. Its chloro group facilitates Suzuki-Miyaura and Buchwald-Hartwig couplings, while the diamine functionality supports diverse functionalization via alkylation or acylation. Bench-stable and readily purified, it functions effectively in multi-step synthesis workflows requiring orthogonality and compatibility with common protecting groups.
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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 : 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: