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Structure of 1931900-04-7
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trans-3-Bromocyclobutane-1-carboxylic acid features a rigid cyclobutane scaffold with stereochemically defined bromide and carboxylic acid groups. This configuration enables predictable reactivity in transition-metal-catalyzed couplings and serves as a key chiral building block for bioactive molecule synthesis.
trans-3-Bromocyclobutane-1-carboxylic acid serves as a versatile building block for cyclobutane-based scaffolds in medicinal chemistry and synthetic methodology. Its stereochemically defined bromide enables reliable SN2 substitutions and palladium-catalyzed coupling reactions, while the carboxylic acid facilitates derivatization via esterification or amide formation. The compound exhibits good bench stability and is readily purified by recrystallization, supporting its use in scalable synthesis workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: