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Structure of 706786-41-6
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This bench-stable phenolic alcohol features a 3,5-difluoro-4-methoxyphenyl scaffold, delivering enhanced electronic and steric control. The methoxy group stabilizes electron density, while the ortho-fluorines enable selective functionalization in synthetic sequences. Ideal for coupling reactions and medicinal chemistry applications requiring halogen-directed derivatization.
(3,5-Difluoro-4-methoxyphenyl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated aromatic scaffolds. Its benzylic alcohol functionality facilitates straightforward derivatization—such as oxidation to carboxylic acids or conversion to esters and ethers—while the ortho-fluorine substituents enhance metabolic stability and modulate electronic properties. The methoxy group provides a handle for further functionalization and contributes favorable lipophilicity. Bench-stable and compatible with standard reaction conditions, it functions effectively in coupling, cyclization, and heterocycle construction 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-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: