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Structure of 163089-34-7
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This silyl ether derivative features a stable tert-butyldimethylsilyl group protecting a hydroxyl moiety, paired with a methoxy-methyl amide functionality. It enables selective O-silylation in complex molecule synthesis, offering reliable protection under standard conditions with minimal side reactivity.
2-(tert-Butyldimethylsilyloxy)-N-methoxy-N-methylacetamide serves as a robust silyl protecting group reagent for alcohols and phenols, enabling selective protection under mild conditions. Its stability toward nucleophiles and common reaction conditions facilitates straightforward deprotection with fluoride sources. The acetyl-derived oxazolidinone moiety enhances solubility and simplifies purification, making it ideal for iterative synthesis workflows in complex molecule assembly.
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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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: