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Structure of 3292-77-1
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2-(Bromoacetyl)-1,3-thiazole features a reactive bromoacetyl group tethered to a heteroaromatic thiazole core, enabling site-specific conjugation in synthetic workflows. This bench-stable reagent integrates readily into peptide and small-molecule derivatization, offering high chemoselectivity under mild conditions.
2-(Bromoacetyl)-1,3-thiazole serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient C–C and C–N bond formation. The bromoacetyl group exhibits high reactivity toward nucleophiles, facilitating rapid functionalization under mild conditions. Its stability under standard bench handling and compatibility with diverse functional groups make it ideal for constructing heterocyclic scaffolds, peptide conjugates, and advanced intermediates in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: