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Structure of 16629-14-4
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2,5-Dichloro-1,3-thiazole is a bench-stable, electron-deficient heterocycle featuring two chlorine substituents at the 2 and 5 positions. This configuration enhances its reactivity in nucleophilic substitution processes, enabling efficient incorporation into complex molecular architectures. The molecule’s rigid, planar structure supports its use as a building block in medicinal chemistry and materials science applications.
2,5-Dichloro-1,3-thiazole serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient construction of bioactive heterocycles. Its dichloro substitution pattern enhances electrophilic reactivity at C2 and C5, facilitating nucleophilic displacement and transition-metal-catalyzed coupling reactions. The compound exhibits good bench stability and compatibility with common functional groups, making it valuable for modular synthesis of pharmaceutical intermediates and agrochemical 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-H312-H315-H319-H332-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: