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Structure of 946607-10-9
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1,3-Di-t-butylbenzimidazolium chloride features a sterically shielded benzimidazolium core with two bulky t-butyl groups flanking the nitrogen atoms. This substitution enhances stability and solubility in organic media while minimizing nucleophilic attack at the cationic center. The chloride counterion enables straightforward anion exchange for tailored reactivity. Ideal for catalytic applications requiring robust, electron-deficient imidazolium platforms under standard bench conditions.
1,3-Di-t-butylbenzimidazolium chloride serves as a robust, bench-stable N-heterocyclic carbene (NHC) precursor with enhanced steric protection from the bulky t-butyl groups. It facilitates efficient metal-free catalysis in cross-coupling and C–H activation reactions, offering high functional group tolerance and ease of handling. The chloride counterion enables straightforward salt formation and purification, making it ideal for synthetic workflows requiring stable, modular benzimidazolium building blocks.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: