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Structure of 68236-23-7
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2-Chloro-6,7-dimethoxyquinoline-3-carbaldehyde features a quinoline core functionalized with chlorine and two methoxy groups at positions 2, 6, and 7, respectively, and an aldehyde group at C3. This electron-deficient scaffold integrates readily into synthetic routes for bioactive molecules, leveraging its polar aldehyde handle and steric profile for selective coupling reactions under standard conditions.
2-Chloro-6,7-dimethoxyquinoline-3-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to quinoline-based scaffolds. Its aldehyde functionality facilitates reductive amination, Ugi-type condensations, and Suzuki-Miyaura coupling reactions. The ortho-chloro and dimethoxy substituents provide enhanced stability and favorable electronic properties for downstream functionalization, while the molecule exhibits excellent bench stability and ease of purification—making it well-suited for high-throughput synthesis and process development workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: