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Structure of 112930-39-9
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3-Bromo-5-isopropylbenzoic acid features a bromine atom at the meta position relative to the carboxylic acid, paired with a sterically hindered isopropyl group para to the bromide. This substitution pattern enhances stability and directs electrophilic functionalization. The compound serves as a key intermediate in synthesizing bioactive molecules and conjugated materials, particularly where electron-deficient aromatic systems are required.
3-Bromo-5-isopropylbenzoic acid serves as a versatile building block for medicinal chemistry and materials science, enabling direct incorporation of bromine and isopropyl functionalities in late-stage functionalization. Its carboxylic acid group facilitates amide coupling, esterification, and metal-catalyzed transformations, while the ortho-bromine supports Suzuki-Miyaura and Stille couplings. The isopropyl substituent enhances lipophilicity and steric profile, offering favorable properties for scaffold diversification. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: