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Structure of 944124-72-5
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2-Chloro-1,3-thiazole-4-carbonitrile features a dual functionalization pattern with chlorine and nitrile groups at adjacent positions on the thiazole ring. This electron-deficient heterocycle serves as a key scaffold for medicinal chemistry applications, enabling direct incorporation into bioactive molecules through nucleophilic substitution or transition-metal-catalyzed coupling reactions.
2-Chloro-1,3-thiazole-4-carbonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to functionalized thiazole scaffolds. Its dual electrophilic sites—chlorine at C2 and nitrile at C4—facilitate sequential nucleophilic substitutions, palladium-catalyzed couplings, and cyclization reactions. The compound exhibits good bench stability and is compatible with common reaction conditions, making it valuable for medicinal chemistry campaigns and API intermediate development.
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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: