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Structure of 348-10-7
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(2-Fluorophenoxy)acetic acid features a fluorinated aromatic ring linked to a carboxylic acid-bearing aliphatic chain, enabling enhanced metabolic stability and targeted bioactivity. This configuration supports efficient integration into agrochemical scaffolds and pharmaceutical intermediates, offering improved membrane permeability and resistance to oxidative degradation under standard conditions.
(2-Fluorophenoxy)acetic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive compounds through established esterification and amidation reactions. Its fluorinated aromatic ring enhances metabolic stability and modulates electronic properties, while the carboxylic acid group facilitates straightforward derivatization. The compound exhibits good bench stability and compatibility with standard purification techniques, making it suitable for use in multi-step synthetic sequences targeting pharmaceutical intermediates and agrochemical scaffolds.
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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: