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Structure of 5059-30-3
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2-Chloro-1H-indole-3-carbaldehyde features a chlorinated indole core with a reactive aldehyde group at the 3-position, enabling direct coupling in C–C bond formation. This electron-deficient scaffold integrates readily into bioactive molecule design, particularly in medicinal chemistry and heterocyclic synthesis workflows.
2-Chloro-1H-indole-3-carbaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient access to indole-based scaffolds. The aldehyde functionality facilitates reductive amination, Grignard additions, and Ugi-type reactions, while the 2-chloro substituent offers orthogonal reactivity for subsequent functionalization. Its bench-stable nature and compatibility with standard purification methods make it well-suited for iterative synthesis workflows in API development and library generation.
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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: