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Structure of 1159186-56-7
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This boronate-bearing arylmethanol features a trifluorinated benzene core with orthogonal functional handles, enabling direct coupling in cross-coupling protocols. The bromo group facilitates Pd-catalyzed transformations, while the hydroxymethyl moiety offers downstream derivatization potential under standard conditions.
(3-Bromo-2,5-difluorophenyl)methanol serves as a versatile building block for Suzuki-Miyaura and Negishi coupling reactions, enabling efficient construction of biaryl and heterocyclic scaffolds. The pendant hydroxymethyl group facilitates derivatization to esters, ethers, or amides, while the bromo and difluoro substituents offer orthogonal functional handles for sequential transformations. Bench-stable and compatible with standard reaction conditions, it supports scalable synthesis in medicinal chemistry and materials science applications.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: