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Structure of 827-01-0
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5-Chloroindole-3-carboxaldehyde features a chlorinated indole core with a reactive aldehyde group at the 3-position, enabling direct coupling in heterocyclic synthesis. This bench-stable derivative integrates readily into bioactive molecule scaffolds, offering enhanced electronic effects and improved solubility for downstream functionalization.
5-Chloroindole-3-carboxaldehyde serves as a versatile building block for the synthesis of biologically active heterocycles and pharmaceutical intermediates. The aldehyde functionality enables efficient coupling reactions, while the chlorinated indole core provides enhanced electronic properties and metabolic stability. Its bench-stable nature and compatibility with standard functional group transformations make it well-suited for medicinal chemistry campaigns and scale-up applications.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: