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Structure of 23077-44-3
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6-Fluoro-1H-indole-3-carboxylic acid features a fluorinated indole core with a carboxylic acid group at the 3-position, enabling direct conjugation or derivatization in synthetic workflows. The electron-withdrawing fluorine substituent enhances metabolic stability and modulates electronic properties, making this scaffold valuable for medicinal chemistry and bioactive molecule development.
6-Fluoro-1H-indole-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of biologically active indole derivatives. Its fluorinated aromatic ring enhances metabolic stability and modulates electronic properties, while the carboxylic acid group facilitates direct coupling reactions or derivatization. The compound exhibits good bench stability and compatibility with standard peptide and heterocyclic coupling protocols, making it well-suited for parallel library synthesis and API development.
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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: