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Structure of 120277-01-2
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4-(2-Bromoethyl)pyridine hydrobromide offers a reactive bromoalkyl handle appended to a pyridine core, enabling efficient coupling in nucleophilic substitution and metal-catalyzed transformations. The hydrobromide salt enhances solubility and stability in polar solvents, simplifying handling in synthetic workflows.
4-(2-Bromoethyl)pyridine hydrobromide serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient construction of nitrogen-containing heterocycles and functionalized alkyl chains. The bromoethyl side chain facilitates nucleophilic substitution reactions, while the pyridinium moiety enhances solubility and stability under standard reaction conditions. This compound is particularly valuable for synthesizing bioactive scaffolds, including those found in medicinal chemistry campaigns requiring controlled alkylation or metal-catalyzed coupling processes. Its bench-stable form simplifies handling and purification in multi-step syntheses.
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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-H335
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Precautionary Statements : P260-P261-P264-P270-P271-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: