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Structure of 180635-74-9
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4-(Trifluoromethyl)benzenepropanol features a trifluoromethyl group that imparts enhanced electron-withdrawing character and metabolic stability. This aromatic alcohol integrates readily into pharmaceutical scaffolds, offering improved lipophilicity and resistance to oxidative degradation under standard conditions.
4-(Trifluoromethyl)benzenepropanol serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive scaffolds through standard functional group transformations. Its trifluoromethyl aryl moiety imparts enhanced metabolic stability and lipophilicity, while the primary alcohol facilitates derivatization via esterification, ether formation, or oxidation to aldehyde. The compound exhibits good bench stability and is compatible with common reaction conditions, making it suitable for both small-scale synthesis and process development 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: