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*For research and further manufacturing use only, not for direct human use.
Structure of 151411-98-2
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2-(Bromomethyl)-1,3,5-trifluorobenzene features a reactive bromomethyl group attached to a trifluorinated aromatic ring, enabling efficient coupling reactions in synthetic chemistry. The electron-deficient benzene core enhances electrophilic reactivity, while the fluorine substituents confer enhanced metabolic stability and lipophilicity. This compound serves as a key building block for pharmaceutical intermediates, agrochemicals, and specialty polymers.
2-(Bromomethyl)-1,3,5-trifluorobenzene serves as a versatile electrophilic building block for nucleophilic substitution reactions, enabling efficient C–C and C–heteroatom bond formation. The trifluoromethylbenzene scaffold imparts enhanced metabolic stability and lipophilicity, making it valuable in medicinal chemistry. Its bromomethyl group exhibits high reactivity under mild conditions, facilitating coupling with amines, thiols, and organometallic reagents. Bench-stable and readily purified by distillation, it functions reliably in multi-step syntheses of fluorinated aromatic compounds and functionalized heterocycles.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H314
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Precautionary Statements : P264-P270-P280-P301+P330+P331-P363-P405-P501
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Lot numbers can be found on the outside label of a product: