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Structure of 121660-37-5
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2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carbaldehyde features a rigid quinoline core functionalized with a cyclopropyl group and a 4-fluorophenyl substituent, enhancing lipophilicity and metabolic stability. The aldehyde handle enables direct coupling in Suzuki-Miyaura and Ullmann reactions, facilitating rapid access to bioactive heterocycles. This scaffold exhibits strong electron-withdrawing character, ideal for conjugated systems in photophysical applications.
2-Cyclopropyl-4-(4-fluorophenyl)quinoline-3-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of quinoline-based scaffolds with defined spatial and electronic properties. The aldehyde functionality facilitates key transformations such as reductive amination, Wittig reactions, and nucleophilic additions, while the cyclopropyl and 4-fluorophenyl substituents enhance metabolic stability and modulate lipophilicity. Its bench-stable crystalline form simplifies handling and purification, supporting scalable applications in target-oriented synthesis.
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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: