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Structure of 952959-39-6
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7-Bromo-5-chloro-1H-indole-2-carboxylic acid features a halogenated indole core with complementary bromo and chloro substituents at the 7- and 5-positions, respectively. This electron-deficient scaffold integrates readily into pharmaceutical intermediates and bioactive molecule frameworks. The carboxylic acid group enables direct coupling reactions or derivatization under standard conditions. Bench-stable and moisture-tolerant, it serves as a robust building block for targeted synthesis in medicinal chemistry and materials science.
7-Bromo-5-chloro-1H-indole-2-carboxylic acid serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling direct incorporation into bioactive scaffolds via standard coupling reactions. The molecule features orthogonal halogen handles (Br at C7, Cl at C5) that facilitate selective cross-coupling, while the carboxylic acid group supports amide formation and derivatization. Bench-stable and readily purified by recrystallization, it functions efficiently in Pd-catalyzed transformations and is compatible with common protecting group strategies in multi-step syntheses.
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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: