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Structure of 101580-96-5
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2-Chloro-4-methyl-5-nitrobenzoic acid features a conjugated aryl core bearing electron-withdrawing nitro and chloro substituents alongside an activating methyl group, enabling selective functionalization. The carboxylic acid moiety provides a robust anchor for peptide coupling or esterification, while the ortho-chloro and para-nitro positions offer sites for palladium-catalyzed cross-coupling reactions. This compound exhibits enhanced stability under standard bench conditions and facilitates access to bioactive heterocycles and pharmaceutical intermediates through modular derivatization pathways.
2-Chloro-4-methyl-5-nitrobenzoic acid serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted heterocycles via standard coupling and cyclization protocols. Its ortho-chloro and meta-nitro groups provide complementary reactivity for selective functionalization, while the carboxylic acid facilitates amidation, esterification, and metal-catalyzed transformations. Bench-stable and readily purified by recrystallization, it supports scalable synthesis of complex scaffolds.
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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 : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: