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Structure of 2939-05-1
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This imidazole derivative features a bromomethyl group enabling efficient functionalization in synthetic workflows. The hydrobromide salt enhances solubility and stability under standard conditions, facilitating use in nucleophilic substitution reactions and the construction of complex heterocyclic architectures.
2-(Bromomethyl)-1H-imidazole hydrobromide serves as a versatile bifunctional building block, enabling efficient installation of both imidazole and bromomethyl functionalities in a single step. Its reactive bromomethyl group facilitates nucleophilic substitution reactions, including etherification, amidation, and coupling with heterocycles, while the protonated imidazole ring enhances solubility and stability under standard synthetic conditions. The compound exhibits excellent bench stability and simplifies purification, making it ideal for modular synthesis of functionalized pharmaceutical intermediates and bioactive scaffolds.
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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#: 1759
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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-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: