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*For research and further manufacturing use only, not for direct human use.
Structure of 395-33-5
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This hydroxyacid features a 4-fluorophenyl group attached to a chiral α-hydroxyacetic backbone, combining enhanced metabolic stability with favorable solubility. The para-fluoro substitution imparts electron-withdrawing character, modulating reactivity in downstream transformations. This bench-stable compound integrates readily into synthetic sequences requiring polar, aromatic functionalities under standard conditions.
2-(4-Fluorophenyl)-2-hydroxyacetic acid serves as a versatile building block for synthesizing bioactive heterocycles and pharmaceutical intermediates. Its ortho-hydroxyacid functionality enables facile cyclization reactions, while the fluorinated aromatic ring enhances metabolic stability and modulates electronic properties. The compound exhibits good bench stability and compatibility with standard protecting group strategies, facilitating downstream functionalization in medicinal chemistry campaigns.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: