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Structure of 1055320-72-3
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7-Chloro-1H-indole-6-carboxylic acid features a chlorinated indole core with a carboxylic acid group at the 6-position, enabling direct conjugation in bioactive molecule synthesis. The electron-deficient aromatic system enhances reactivity in coupling reactions, while the bench-stable functionality supports efficient integration into pharmaceutical and agrochemical scaffolds under standard conditions.
7-Chloro-1H-indole-6-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into bioactive heterocycles via standard coupling reactions. Its ortho-chloro substituent enhances electrophilic reactivity and facilitates downstream functionalization, while the carboxylic acid group supports efficient amide and ester formation. The compound exhibits good bench stability and compatibility with common purification methods, making it well-suited for iterative synthesis campaigns targeting kinase inhibitors and CNS-active scaffolds.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: