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Structure of 14035-33-7
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This sterically shielded ketone features a para-hydroxyphenyl core flanked by bulky tert-butyl groups, conferring exceptional stability and resistance to oxidation. The electron-rich aromatic system enables selective functionalization in synthetic transformations.
1-(3,5-Di-tert-butyl-4-hydroxyphenyl)ethan-1-one serves as a stable, bench-accessible aryl ketone scaffold with enhanced solubility and steric protection from the bulky tert-butyl groups. The phenolic hydroxyl group enables direct functionalization or derivatization in standard coupling reactions, while the ketone functionality facilitates nucleophilic additions and enolate chemistry. This compound functions effectively as a building block for antioxidant-related heterocycles and provides robust stability under routine handling conditions.
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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 : H315-H319-H335-H413
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Precautionary Statements : P261-P264-P271-P273-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: