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Structure of 50916-55-7
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This bromoacetyl-substituted benzonitrile delivers a reactive handle for site-specific conjugation, combining a nucleophilic nitrile group with a labile bromoacetyl moiety. The electrophilic acyl bromide functionality enables efficient coupling under mild conditions, facilitating the integration of aromatic scaffolds into bioconjugates and functional materials.
3-(2-Bromoacetyl)benzonitrile serves as a versatile bifunctional building block for medicinal chemistry and heterocycle synthesis. The bromoacetyl group enables nucleophilic substitution reactions, while the ortho-cyano group facilitates cyclization or transition metal-catalyzed coupling. Its bench-stable crystalline form supports straightforward handling and purification, making it well-suited for modular synthesis of bioactive scaffolds and API intermediates.
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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#: 3263
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302+H312+H332-H314
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P330+P331-P302+P352-P304+P340-P330-P362+P364-P363-P405-P501
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Lot numbers can be found on the outside label of a product: