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Structure of 635-21-2
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2-Amino-5-chlorobenzoic acid features a chlorinated aromatic ring with strategically positioned amino and carboxylic acid groups, enabling direct integration into pharmaceutical intermediates. The electron-withdrawing chlorine enhances reactivity in coupling processes, while the amino functionality offers facile derivatization potential under mild conditions. This compound serves as a key scaffold for bioactive molecule synthesis.
2-Amino-5-chlorobenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzimidazoles and other heterocyclic scaffolds via condensation reactions. Its ortho-amino and carboxylic acid functionalities offer complementary reactivity for peptide coupling, cyclization, and metal-catalyzed transformations. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring functional group compatibility and structural precision.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: