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Structure of 20034-50-8
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4-Cyclopropylbenzaldehyde features a cyclopropyl group at the para position of the benzaldehyde ring, imparting enhanced lipophilicity and conformational rigidity. This structural motif enables efficient integration into bioactive scaffolds and facilitates directed functionalization in synthetic pathways. The aldehyde functionality offers high reactivity for nucleophilic addition and condensation reactions under standard conditions.
4-Cyclopropylbenzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling the synthesis of bioactive heterocycles and functionalized aromatics. Its aldehyde functionality facilitates efficient imine formation, reductive amination, and transition-metal-catalyzed coupling reactions. The cyclopropyl group imparts favorable lipophilic character and conformational rigidity, enhancing metabolic stability in target molecules. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step syntheses.
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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: