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Structure of 2302-88-7
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2-Acetylhydrazinecarbothioamide features a hydrazinecarbothioamide core with an acetyl substituent, delivering enhanced reactivity in heterocyclic synthesis. This bench-stable compound integrates readily into sulfur-containing scaffolds, offering efficient access to functionalized imidazoles and triazoles under standard conditions.
2-Acetylhydrazinecarbothioamide serves as a versatile building block in heterocyclic synthesis, enabling efficient access to thiazole and imidazole scaffolds through condensation and cyclization reactions. Its dual hydrazine and thiocarbonyl functionalities exhibit excellent stability under standard bench conditions and tolerate a range of functional groups, facilitating straightforward purification and integration into multi-step synthetic sequences.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: