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Structure of 37859-43-1
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2-(Chloromethyl)benzothiazole features a reactive chloromethyl group appended to the benzothiazole core, enabling efficient functionalization in synthetic transformations. This electrophilic handle facilitates coupling reactions under mild conditions, integrating readily into complex molecular architectures. The compound exhibits good stability and solubility in common organic solvents, supporting its use in medicinal chemistry and materials synthesis workflows.
2-(Chloromethyl)benzothiazole serves as a versatile electrophilic building block in synthetic organic chemistry, enabling efficient C–C and C–heteroatom bond formation. Its chloromethyl group readily participates in nucleophilic substitution reactions under mild conditions, facilitating the construction of complex benzothiazole derivatives. The molecule exhibits good bench stability and compatibility with common functional groups, making it well-suited for iterative synthesis workflows in medicinal chemistry and materials science.
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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#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: