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Structure of 79025-26-6
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Methyl 2-amino-5-chloro-4-methoxybenzoate features a strategically positioned amino group flanked by electron-withdrawing chlorine and methoxy substituents, enabling selective coupling reactions in medicinal chemistry. This bench-stable derivative integrates readily into complex heterocycles and serves as a key intermediate for bioactive molecule synthesis under standard conditions.
Methyl 2-amino-5-chloro-4-methoxybenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, quinoline derivatives, and other heterocyclic scaffolds. Its compatibility with standard coupling reactions, robust bench stability, and tolerance to diverse functional groups facilitate streamlined downstream transformations. The strategically positioned amino, chloro, and methoxy substituents support sequential derivatization for targeted molecular design.
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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: