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Structure of 16265-04-6
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2-Chloro-1H-imidazole is a bench-stable, moisture-tolerant heterocycle featuring a chlorine substituent at the 2-position, enabling direct functionalization in cross-coupling and electrophilic substitution reactions. This electron-deficient imidazole serves as a robust scaffold for synthesizing bioactive molecules and advanced intermediates in medicinal chemistry and materials science.
2-Chloro-1H-imidazole serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted imidazoles via nucleophilic displacement or transition-metal-catalyzed coupling. Its bench-stable nature and compatibility with diverse functional groups facilitate straightforward incorporation into complex molecular architectures. The chloride moiety provides a reliable handle for C–C and C–heteroatom bond formation, making it a practical reagent for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: