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Structure of 79025-82-4
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2-Amino-5-chloro-4-methoxybenzoic acid features a strategically positioned amino group and electron-withdrawing chlorine, enabling precise tuning of reactivity in pharmaceutical intermediates. The methoxy substituent enhances solubility and stability under standard conditions. This scaffold integrates readily into bioactive molecules requiring balanced polarity and metabolic resistance.
2-Amino-5-chloro-4-methoxybenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzimidazoles and other heterocyclic scaffolds. Its ortho-amino and carboxylic acid functionalities facilitate efficient coupling reactions and cyclizations under standard conditions. The chloro and methoxy groups provide regioselective handles for further functionalization, while the compound exhibits good bench stability and ease of purification, making it well-suited for scalable synthesis workflows.
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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 : H319
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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: