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*For research and further manufacturing use only, not for direct human use.
Structure of 2557-13-3
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Methyl 3-(trifluoromethyl)benzoate features a trifluoromethyl group that imparts strong electron-withdrawing character, enhancing reactivity in nucleophilic aromatic substitution. This bench-stable ester integrates readily into synthetic sequences requiring polar, fluorinated aromatic intermediates.
Methyl 3-(trifluoromethyl)benzoate serves as a versatile building block in medicinal chemistry and synthetic organic research. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, while the ester functionality enables straightforward derivatization via hydrolysis, reduction, or coupling reactions. The compound exhibits good bench stability and is compatible with a range of standard reaction conditions, facilitating efficient access to functionalized aromatic scaffolds used in API development.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 3272
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H315-H319-H335
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Precautionary Statements : P210-P240-P241-P280-P370+P378
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Lot numbers can be found on the outside label of a product: