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Structure of 15965-55-6
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2-Chloro-7-nitro-1H-benzo[d]imidazole features a fused bicyclic core with complementary electron-deficient character, enabling efficient coupling in cross-coupling transformations. The ortho-chloro and para-nitro substituents provide orthogonal reactivity for sequential functionalization, while the bench-stable imidazole scaffold ensures reliable handling under standard conditions.
2-Chloro-7-nitro-1H-benzo[d]imidazole serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of bioactive scaffolds. Its orthogonal functionalization profile—combining electrophilic chlorine and strongly electron-withdrawing nitro groups—facilitates palladium-catalyzed cross-coupling and directed metallation. The compound exhibits excellent bench stability and compatibility with standard purification protocols, making it well-suited for medicinal chemistry campaigns and process-scale applications.
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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 : 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: