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Structure of 1192027-04-5
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This formimidamide features a unique (E)-configured imine linkage paired with a 3-thioxo-3H-1,2,4-dithiazol-5-yl moiety, delivering enhanced stability and reactivity. The dimethyl substitution ensures solubility in common organic solvents, while the electron-deficient dithiazole ring facilitates nucleophilic addition reactions. This compound serves as a selective building block for heterocyclic synthesis and functional material development under standard bench conditions.
(E)-N,N-Dimethyl-N'-(3-thioxo-3H-1,2,4-dithiazol-5-yl)formimidamide serves as a versatile building block in heterocyclic synthesis, enabling efficient access to thiazole and dithiazole frameworks. Its stable (E)-configuration and tolerance to common functional groups facilitate reliable incorporation into complex molecular architectures. The molecule functions as a key intermediate in the construction of sulfur-rich heterocycles relevant to medicinal chemistry and materials science.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: