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Structure of 340-05-6
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1-Phenyl-2,2,2-trifluoroethanol features a trifluoromethyl group that imparts strong electron-withdrawing character and enhanced metabolic stability. This bench-stable compound integrates readily into fluorinated scaffolds for medicinal chemistry applications. The phenyl moiety provides π-conjugation, enabling efficient incorporation into bioactive molecules. Its moisture-tolerant handling simplifies use in multi-step syntheses.
1-Phenyl-2,2,2-trifluoroethanol serves as a stable, bench-ready building block for fluorinated aromatic systems. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry workflows. The molecule readily participates in nucleophilic substitution and coupling reactions, enabling efficient access to functionalized aryl trifluoromethyl compounds. Its crystalline solid form facilitates handling and purification, supporting scalable synthesis.
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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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: