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Structure of 32122-23-9
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1-Bromocyclobutanecarboxylic acid features a cyclobutanecarboxylic acid scaffold bearing a bromine atom at the adjacent carbon, enabling direct functionalization in synthetic transformations. The carboxylic acid group provides polarity and reactivity for coupling reactions, while the strained cyclobutane ring enhances electrophilic character. This compound serves as a key intermediate in medicinal chemistry and materials science, facilitating access to cyclic frameworks with defined stereochemistry under standard conditions.
1-Bromocyclobutanecarboxylic acid serves as a versatile building block for cyclobutane-containing scaffolds in medicinal chemistry and materials science. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates derivatization via amide, ester, or acyl chloride formation. Its stability under standard bench conditions and compatibility with common protecting groups make it well-suited for multi-step synthesis.
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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#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: