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*For research and further manufacturing use only, not for direct human use.
Structure of 16079-88-2
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This bromochloroimidazolidinedione delivers a dual halogen handle for orthogonal functionalization, combining reactive bromine at C1 with electrophilic chlorine at C3. The sterically shielded 5,5-dimethyl substitution enhances stability under standard conditions, enabling reliable use in late-stage diversification and synthetic transformations.
1-Bromo-3-chloro-5,5-dimethylimidazolidine-2,4-dione serves as a versatile dihalogenated heterocyclic building block for the synthesis of imidazolidinone-based scaffolds. Its reactivity enables selective nucleophilic substitution at the bromo position while retaining stability under standard bench conditions. The molecule functions effectively in coupling reactions and facilitates the construction of complex heterocycles relevant to medicinal chemistry, with excellent functional group tolerance and straightforward purification.
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GHS Pictogram :
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GHS No : GHS03,GHS05
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Signal Word : Danger
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UN#: 3085
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Class : 5.1 (8)
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Packing Group : Ⅱ
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Hazard Statements : H272-H302+H312+H332-H314
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Precautionary Statements : P210-P220-P260-P264-P270-P273-P280-P301+P330+P331-P304+P340-P391-P405-P501
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Lot numbers can be found on the outside label of a product: