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Structure of 1805773-37-8
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This difluoromethylthio-substituted isoindoline-1,3-dione features a uniquely reactive thioether moiety flanked by electron-deficient carbonyl groups. The difluoromethylthio handle enables selective functionalization in synthetic transformations, offering enhanced stability under standard conditions while maintaining high reactivity in cross-coupling and cycloaddition processes.
2-((Difluoromethyl)thio)isoindoline-1,3-dione serves as a versatile building block in medicinal chemistry, enabling the introduction of a difluoromethylthio group—a fluorinated electrophilic handle—into complex scaffolds. Its isoindoline-1,3-dione core provides structural rigidity and favorable polarity for downstream functionalization. The molecule exhibits bench stability, tolerates common reaction conditions, and facilitates access to bioactive heterocycles through standard coupling and cyclization protocols.
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335-H410
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Precautionary Statements : P261-P264-P270-P271-P273-P280-P302+P352-P304+P340-P330-P362+P364-P391-P405-P501
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Lot numbers can be found on the outside label of a product: