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77943-39-6

(4R,5S)-4-Methyl-5-phenyloxazolidin-2-one

Catalog#: AR003CLZ  |   CAS#: 77943-39-6  |   MDL#: MFCD00010845  |   MF: C10H11NO2  |   MW: 177.1998

Packsize Purity Price Availability Quantity
1g 98% $5.00 Global Stock Buy Now Add To Cart
5g 98% $19.00 Global Stock Buy Now Add To Cart
10g 98% $37.00 Global Stock Buy Now Add To Cart
25g 98% $87.00 Global Stock Buy Now Add To Cart
100g 98% $345.00 Global Stock Buy Now Add To Cart
500g 98% $1,377.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003CLZ
Chemical Name (4R,5S)-4-Methyl-5-phenyloxazolidin-2-one
CAS Number 77943-39-6
Molecular Formula C10H11NO2
Molecular Weight 177.1998
MDL Number MFCD00010845
SMILES C[C@H]1NC(=O)O[C@H]1c1ccccc1

(4R,5S)-4-Methyl-5-phenyloxazolidin-2-one is a versatile chiral building block commonly used in chemical synthesis for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique stereochemistry, this compound serves as a valuable intermediate in the preparation of complex molecules with specific chirality and biological activity.In chemical synthesis, (4R,5S)-4-Methyl-5-phenyloxazolidin-2-one plays a crucial role as a key starting material for the synthesis of enantiomerically pure compounds. Its presence in synthetic pathways allows chemists to control the stereochemistry of reactions, leading to the formation of highly selective and biologically active products. This compound's chirality influences the outcomes of reactions, making it a valuable tool for designing efficient synthetic routes.By incorporating (4R,5S)-4-Methyl-5-phenyloxazolidin-2-one into synthetic schemes, chemists can access a wide range of molecular structures that are essential for drug discovery, material science, and other fields requiring specialized compounds. Its strategic placement in chemical transformations enables the creation of complex molecules with precise spatial arrangements, making it a sought-after reagent in organic synthesis.In summary, (4R,5S)-4-Methyl-5-phenyloxazolidin-2-one serves as a fundamental building block in chemical synthesis, facilitating the construction of chiral molecules and enabling the preparation of advanced intermediates with specific stereochemistry. Its role in synthetic methodologies highlights its importance in the development of novel compounds with targeted properties and applications.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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