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Structure of 5202-89-1
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Methyl 2-amino-5-chlorobenzoate features a para-chloro-substituted aromatic ring paired with an ortho-amino group, enabling selective coupling reactions in medicinal chemistry. This bench-stable derivative integrates readily into heterocyclic scaffolds and serves as a key intermediate for bioactive compound synthesis.
Methyl 2-amino-5-chlorobenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, quinolines, and other heterocyclic scaffolds. The ortho-amino and meta-chloro groups provide complementary reactivity for sequential functionalization, while the methyl ester facilitates straightforward manipulation via hydrolysis or coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in standard synthetic 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 : 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: