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Structure of 38642-74-9
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2-Cyanophenothiazine features a phenothiazine core functionalized with a cyano group at the 2-position, delivering enhanced electron-withdrawing character. This structural motif enables efficient charge transfer in organic semiconductors and facilitates incorporation into redox-active materials for optoelectronic applications. The compound exhibits good stability under ambient conditions and integrates readily into molecular architectures requiring tunable electronic properties.
2-Cyanophenothiazine serves as a versatile building block in synthetic organic chemistry, enabling the construction of functionalized heterocycles through palladium-catalyzed cross-coupling reactions. Its electron-rich phenothiazine core and nitrile group offer orthogonal reactivity, facilitating downstream derivatization while maintaining bench stability. The molecule functions effectively in Suzuki, Sonogashira, and Buchwald–Hartwig coupling protocols, making it valuable for developing advanced materials and pharmaceutical intermediates.
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GHS Pictogram :
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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: