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Structure of 84627-04-3
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This biphenyl-based carboxylic acid features a hydroxyl group at the 6-position of the phenyl ring, enhancing solubility and enabling hydrogen bonding. The para-substituted benzoic acid moiety provides a rigid, electron-deficient platform ideal for conjugate addition reactions and molecular scaffold integration in medicinal chemistry.
2-(6-Hydroxy-[1,1'-biphenyl]-3-carbonyl)benzoic acid serves as a versatile building block for constructing biaryl-containing scaffolds in medicinal chemistry and materials science. The molecule combines a carboxylic acid functionality with a phenolic hydroxyl group, enabling diverse derivatization via amide, ester, or ether formation. Its biphenyl core offers structural rigidity and π-conjugation, while the ortho-carbonyl substitution pattern supports controlled reactivity in coupling and cyclization reactions. This compound demonstrates bench stability and compatibility with standard purification methods, facilitating integration into multi-step synthetic sequences.
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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-H319-H412
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Precautionary Statements : P264-P270-P273-P280-P330-P501
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Lot numbers can be found on the outside label of a product: