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Structure of 1121-83-1
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5,5-Dimethyl-1,3-oxazolidin-2-one delivers a stable, moisture-tolerant heterocyclic scaffold ideal for coupling reactions in synthetic and medicinal chemistry. Its electron-deficient carbonyl moiety enables efficient nucleophilic addition, while the sterically hindered dimethyl substitution enhances kinetic stability under standard conditions.
5,5-Dimethyl-1,3-oxazolidin-2-one serves as a stable, bench-ready chiral synthon for asymmetric synthesis, enabling efficient enantioselective transformations via its reactive carbonyl and nitrogen functionalities. Its rigid cyclic structure facilitates stereoselective additions and functions as a key building block in the construction of heterocyclic scaffolds. The dimethyl substitution enhances solubility and stability, simplifying purification and handling in multistep sequences.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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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-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: