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Structure of 1204-60-0
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1,1'-Biphenyl]-3-carbaldehyde features a rigid biphenyl scaffold linked to an aldehyde functional group, enabling direct integration into Suzuki-Miyaura coupling reactions. The carbonyl moiety serves as a handle for downstream derivatization, including imine formation and reductive amination. This electron-deficient aldehyde exhibits enhanced stability under standard bench conditions and facilitates the synthesis of conjugated molecular architectures in organic electronics and medicinal chemistry applications.
[1,1'-Biphenyl]-3-carbaldehyde serves as a versatile building block in organic synthesis, enabling efficient construction of biaryl-containing scaffolds via standard coupling reactions. Its aldehyde functionality facilitates nucleophilic additions, imine formation, and oxidation to the corresponding carboxylic acid. The molecule exhibits good bench stability and is compatible with a range of functional groups, making it suitable for iterative synthesis workflows 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-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: