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Structure of 87954-60-7
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1,3-Dimethylimidazolidin-2-imine hydrochloride serves as a bench-stable nitrogen source in catalytic transformations. This imidazolidinium salt features a rigid heterocyclic core with two methyl groups that enhance solubility and electronic modulation. The hydrochloride counterion ensures stability under ambient conditions while enabling efficient proton transfer in asymmetric synthesis.
1,3-Dimethylimidazolidin-2-imine hydrochloride serves as a stable, bench-ready nitrogen heterocycle that facilitates efficient nucleophilic catalysis in amide bond formation and acyl transfer reactions. Its enhanced solubility and functional group tolerance enable reliable performance in peptide coupling and late-stage functionalization workflows. The imidazolidinone scaffold provides a robust platform for building bioactive molecules and serves as a versatile intermediate in medicinal chemistry synthesis.
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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: