(4R)-3-[((1S,2S)-2-Hydroxy-3-cyclopenten-1-yl)carbonyl]-4-(phenylMethyl)-1,3-oxazolidin-2-one
95%
- Product Code: 82073
CAS:
324741-99-3
| Molecular Weight: | 287.31 g./mol | Molecular Formula: | C₁₆H₁₇NO₄ |
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| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral auxiliary or building block in the preparation of complex molecules. Its structure, featuring a cyclopentene ring and an oxazolidinone moiety, makes it valuable for inducing stereoselectivity in asymmetric reactions. It is often employed in the synthesis of pharmaceuticals, where precise control over the three-dimensional arrangement of atoms is crucial for the biological activity of the final product. Additionally, it can be used in the development of agrochemicals and other fine chemicals that require high enantiomeric purity. Its unique stereochemistry also makes it a useful tool in academic research for studying reaction mechanisms and developing new synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £698.59 |
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(4R)-3-[((1S,2S)-2-Hydroxy-3-cyclopenten-1-yl)carbonyl]-4-(phenylMethyl)-1,3-oxazolidin-2-one
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral auxiliary or building block in the preparation of complex molecules. Its structure, featuring a cyclopentene ring and an oxazolidinone moiety, makes it valuable for inducing stereoselectivity in asymmetric reactions. It is often employed in the synthesis of pharmaceuticals, where precise control over the three-dimensional arrangement of atoms is crucial for the biological activity of the final product. Additionally, it can be used in the development of agrochemicals and other fine chemicals that require high enantiomeric purity. Its unique stereochemistry also makes it a useful tool in academic research for studying reaction mechanisms and developing new synthetic methodologies.
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