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*For research and further manufacturing use only, not for direct human use.
Structure of 398-36-7
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4-(Trifluoromethyl)-1,1'-biphenyl features a trifluoromethyl group appended to a biphenyl scaffold, delivering enhanced electron-withdrawing character and improved metabolic stability. This structural motif enables robust integration into pharmaceutical intermediates and functional materials, particularly where halogenated aromatic systems are required.
4-(Trifluoromethyl)-1,1'-biphenyl serves as a valuable building block in the synthesis of functionalized biaryls and pharmaceutical intermediates. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, while the biphenyl core enables robust coupling reactions via Suzuki-Miyaura and Stille protocols. The compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for scale-up in medicinal chemistry campaigns.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: