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Structure of 6092-47-3
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Ethyl (2-chloroacetyl)carbamate serves as a key acylating agent in synthetic organic chemistry, featuring a reactive chloroacetyl moiety that enables efficient amide bond formation. This bench-stable reagent integrates readily into peptide synthesis and functional group transformations, offering high chemoselectivity under mild conditions.
Ethyl (2-chloroacetyl)carbamate serves as a versatile acylating agent in synthetic organic chemistry, enabling efficient introduction of the chloroacetyl group under mild conditions. Its stability under standard bench handling and compatibility with diverse functional groups make it particularly useful for selective derivatization of nucleophiles, including amines and alcohols. The molecule functions as a key building block in the synthesis of heterocyclic scaffolds and peptide analogs, offering predictable reactivity and straightforward purification.
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GHS Pictogram :
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GHS No : GHS06,GHS08
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: