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Structure of 3652-92-4
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1,3-Dimethyl-2-phenylbenzimidazoline features a rigid, electron-rich benzimidazole core with steric protection from methyl groups at the 1- and 3-positions. The para-substituted phenyl ring enhances planarity and π-conjugation, enabling stable charge delocalization. This bench-stable heterocycle integrates readily into redox-active systems and serves as a robust scaffold for ligand design in catalytic applications.
1,3-Dimethyl-2-phenylbenzimidazoline serves as a stable, bench-ready building block for the synthesis of functionalized benzimidazole scaffolds. Its ortho-quinone-like reactivity enables efficient coupling with electrophiles and facilitates transition-metal-catalyzed transformations. The methyl groups enhance solubility and simplify purification, while the phenyl substituent provides structural rigidity and compatibility in multi-step synthetic sequences.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: