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Structure of 90035-34-0
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4'-Trifluoromethylbiphenyl-4-carboxaldehyde features a rigid biphenyl scaffold bearing a trifluoromethyl group at the para position and a reactive aldehyde handle at the terminal phenyl ring. This electron-deficient aldehyde integrates readily into Suzuki-Miyaura coupling sequences and serves as a key building block for conjugated materials in organic electronics. The trifluoromethyl moiety enhances metabolic stability and lipophilicity, improving performance in functional molecular architectures.
4'-Trifluoromethylbiphenyl-4-carboxaldehyde serves as a versatile building block for the synthesis of functionalized biaryl scaffolds and heterocyclic systems. Its aldehyde functionality enables efficient imine formation, reductive amination, and transition-metal-catalyzed coupling reactions. The trifluoromethyl group enhances metabolic stability and modulates electronic properties, making it valuable in medicinal chemistry lead optimization. Bench-stable and compatible with standard purification methods, it facilitates scalable synthesis in industrial R&D workflows.
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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: