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Structure of 1349171-53-4
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Methyl 4-formyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate features a boronate ester group paired with an aldehyde functionality, enabling efficient cross-coupling reactions. The tetramethyl-substituted dioxaborolane enhances stability and reactivity under standard conditions. This bifunctional building block integrates seamlessly into Suzuki-Miyaura coupling workflows, delivering precise structural control in complex molecule synthesis.
Methyl 4-formyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate serves as a versatile Suzuki-Miyaura coupling building block, enabling efficient construction of biaryl and heteroaryl scaffolds. The boronate ester group offers excellent stability and functional group tolerance, while the aldehyde functionality supports orthogonal transformations including reductive amination and Wittig reactions. This dual-functional molecule facilitates streamlined synthesis of complex molecular architectures in medicinal chemistry and materials science.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: