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*For research and further manufacturing use only, not for direct human use.
Structure of 59394-27-3
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7-Chloroquinoline-2-carbaldehyde delivers a potent electron-deficient scaffold for synthetic and medicinal chemistry applications. This bench-stable aldehyde integrates readily into conjugate addition and condensation reactions, enabling efficient access to functionalized quinoline derivatives under standard conditions.
7-Chloroquinoline-2-carbaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of quinoline-based scaffolds. Its aldehyde functionality facilitates nucleophilic addition, reductive amination, and condensation reactions, while the chloro substituent offers orthogonal reactivity for further functionalization. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for medicinal chemistry campaigns and process development.
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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
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Precautionary Statements : P261-P280-P304+P340
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Lot numbers can be found on the outside label of a product: