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Structure of 1192-81-0
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This oxadiazole derivative features a chloromethyl group enabling direct functionalization in synthetic workflows. The 3-methyl substitution enhances stability while maintaining reactivity, making it suitable for conjugation strategies in medicinal chemistry and probe development.
5-(Chloromethyl)-3-methyl-1,2,4-oxadiazole serves as a versatile bifunctional building block, enabling efficient incorporation of both oxadiazole and chloromethyl moieties into complex molecular architectures. The chloromethyl group facilitates nucleophilic substitution reactions, while the stable 1,2,4-oxadiazole core provides enhanced metabolic resistance and polarity modulation—key attributes in medicinal chemistry lead optimization. Its bench-stable solid form supports straightforward handling and purification in standard synthetic 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#: 3265
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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-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: