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Structure of 1000804-51-2
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This boronate moiety integrates seamlessly into Suzuki-Miyaura coupling reactions, delivering robust yields under standard conditions. The para-cyanophenyl group enhances electron-withdrawing character, while the methylpropanoic acid side chain provides steric bulk and solubility in common organic solvents.
2-(4-Cyanophenyl)-2-methylpropanoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of biologically active heterocycles and pharmaceutical scaffolds. Its benzonitrile functionality facilitates coupling reactions and cyclization processes, while the sterically hindered α-methylpropanoic acid moiety offers enhanced metabolic stability. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis campaigns in drug discovery.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H331
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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: