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Structure of 171879-99-5
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4-Chloro-6-methyl-7-azaindole is a bench-stable, electron-deficient heterocycle featuring a chlorinated aryl moiety and a methyl-substituted pyridine ring. This structural motif enables efficient coupling in cross-coupling reactions and serves as a key scaffold in medicinal chemistry for targeted kinase inhibition and fluorescent probe development.
4-Chloro-6-methyl-7-azaindole serves as a versatile building block in medicinal chemistry, enabling efficient construction of bioactive heterocycles. Its chlorine substituent facilitates palladium-catalyzed cross-coupling reactions, while the methyl group enhances metabolic stability. The 7-azaindole core provides favorable solubility and hydrogen-bonding capacity, making it valuable for scaffold diversity in drug discovery programs.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: