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Structure of 26478-16-0
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2-(2-Bromoethyl)thiophene features a bromoethyl side chain attached to the thiophene ring, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. This configuration supports efficient derivatization for synthetic organic chemistry applications. The molecule exhibits high reactivity at the bromine site with minimal steric hindrance, facilitating rapid incorporation into complex molecular architectures under standard conditions.
2-(2-Bromoethyl)thiophene serves as a versatile bifunctional building block for the synthesis of heterocyclic scaffolds and bioactive molecules. The bromoethyl side chain enables facile nucleophilic substitution, while the thiophene core provides a stable, electron-rich platform for cross-coupling reactions. Its bench-stable nature and compatibility with diverse functional groups make it ideal for iterative synthetic sequences in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-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: