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Structure of 6627-53-8
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5-Chloro-2-nitroanisole features a chlorinated aromatic ring with complementary electron-withdrawing nitro and electron-donating methoxy groups, enabling selective cross-coupling reactions under standard conditions. This bench-stable derivative delivers precise regiocontrol in C–C bond formation, particularly valuable in medicinal chemistry scaffolds.
5-Chloro-2-nitroanisole serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted heterocycles and aromatic scaffolds. Its ortho-nitro and para-chloro functionalities offer complementary reactivity for sequential functionalization—particularly in palladium-catalyzed coupling reactions and nucleophilic substitution processes. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for scalable synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS07,GHS08
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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-H350
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Precautionary Statements : P264-P270-P280-P280
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Lot numbers can be found on the outside label of a product: