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*For research and further manufacturing use only, not for direct human use.
Structure of 372-20-3
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3-Fluorophenol serves as a key building block in pharmaceutical and agrochemical synthesis, offering a reactive phenolic hydroxyl group flanked by a fluorine atom at the meta position. This combination imparts enhanced metabolic stability and modulates electronic properties, enabling efficient incorporation into bioactive scaffolds under standard conditions.
3-Fluorophenol serves as a versatile building block in medicinal chemistry and materials science, enabling efficient functionalization via electrophilic substitution and transition-metal-catalyzed coupling reactions. Its fluorinated aromatic core provides enhanced metabolic stability and modulated electronic properties, while the phenolic hydroxyl group facilitates straightforward derivatization through etherification, esterification, or direct metalation. Bench-stable and compatible with common protecting group strategies, it functions reliably in multi-step syntheses of pharmaceutical intermediates and specialty polymers.
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2922
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Class : 8 (6.1)
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Packing Group : Ⅲ
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Hazard Statements : H227-H301+H311+H331-H314-H412
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Precautionary Statements : P210-P260-P261-P264-P270-P271-P273-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P330-P361+P364-P363-P370+P378-P403-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: