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Structure of 21521-87-9
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2-Chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide features a chloroacetyl group linked to a 5-methyl-1,3,4-thiadiazole scaffold, delivering enhanced reactivity and stability. This configuration enables efficient coupling in heterocyclic synthesis, particularly for constructing bioactive amide derivatives. The molecule exhibits favorable solubility in common organic solvents and maintains bench stability under standard conditions.
2-Chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted thiadiazole derivatives. Its chloroacetyl moiety facilitates nucleophilic substitution and condensation reactions under mild conditions, offering high functional group tolerance and bench stability. The molecule functions as a key intermediate in the construction of bioactive scaffolds relevant to agrochemical and medicinal chemistry applications.
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GHS Pictogram :
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GHS No : GHS05
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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 : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P264-P270-P271-P280-P304+P340-P330-P331-P363-P501
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Lot numbers can be found on the outside label of a product: