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Structure of 886369-06-8
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This thiazole-based carboxylic acid integrates a 3-fluorophenyl group at the 2-position, delivering enhanced electron-withdrawing character and improved metabolic stability. The conjugated system supports efficient coupling in amide bond formation, while the fluorine substituent enhances membrane permeability and target engagement. This scaffold serves as a key building block for bioactive molecule development.
2-(3-Fluorophenyl)-1,3-thiazole-4-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through standard coupling reactions. Its robust bench stability and tolerance to diverse functional groups facilitate efficient synthesis of pharmaceutical intermediates. The carboxylic acid functionality supports direct derivatization or salt formation, enhancing solubility and processability in API development workflows.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: