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Structure of 347372-90-1
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Allyl (2-bromoethyl)carbamate features a reactive allyl group paired with a bromoethyl carbamate moiety, enabling efficient conjugation in synthetic workflows. This bifunctional reagent integrates seamlessly into click chemistry and peptide modification strategies, offering high chemoselectivity under mild conditions. The molecule's stability facilitates handling while maintaining reactivity for downstream transformations.
Allyl (2-bromoethyl)carbamate serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient introduction of both allyl and bromoethyl functionalities. It functions as a protected amine synthon with orthogonal reactivity, facilitating subsequent transformations such as nucleophilic substitution, palladium-catalyzed coupling, and ring-opening reactions. The allyl group allows for convenient removal via Pd(0)-mediated deprotection, while the bromoethyl moiety supports further functionalization through SN2 processes. Its stability under standard bench conditions and compatibility with diverse reaction environments make it well-suited for complex molecule synthesis, including peptide analogs and heterocyclic scaffolds.
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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: