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Structure of 1260666-60-1
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Methyl 6-amino-4-chloronicotinate features a strategically positioned amino group flanking a chlorinated pyridine core, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative supports efficient derivatization in synthetic routes targeting bioactive compounds and functional materials.
Methyl 6-amino-4-chloronicotinate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the amino and ester positions. Its electron-deficient pyridine core facilitates palladium-catalyzed cross-coupling reactions, while the amino group offers straightforward derivatization via acylation, alkylation, or diazotization. The compound exhibits excellent bench stability and is readily purified by crystallization or flash chromatography, making it well-suited for scalable synthesis of heterocyclic scaffolds and API intermediates.
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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: