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Structure of 934241-78-8
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4-Fluoro-3-hydroxybenzyl alcohol features a hydroxyl group flanked by electron-withdrawing fluorine and aromatic ring functionalities, enabling direct functionalization in synthetic sequences. This bench-stable phenolic derivative integrates readily into bioactive molecule scaffolds, offering controlled polarity and hydrogen-bonding capacity for medicinal chemistry applications.
4-Fluoro-3-hydroxybenzyl alcohol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the phenolic hydroxyl and benzylic alcohol sites. Its ortho-fluoro substituent enhances metabolic stability and facilitates downstream coupling reactions. The molecule exhibits excellent bench stability, ease of purification, and compatibility with standard protecting group strategies, making it well-suited for the synthesis of bioactive heterocycles and API intermediates.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: