Methyl (S)-4-Benzyl-5-oxomorpholine-3-carboxylate
≥97%
- Product Code: 57169
CAS:
1235181-00-6
| Molecular Weight: | 249.26 g./mol | Molecular Formula: | C₁₃H₁₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11501467 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the production of various bioactive molecules, including those with potential therapeutic applications. Its structural features make it valuable for constructing complex morpholine derivatives, which are often explored for their pharmacological properties, such as enzyme inhibition or receptor modulation. Additionally, it is employed in research settings to study stereochemistry and reaction mechanisms due to its chiral center. Its role in medicinal chemistry is significant, as it contributes to the synthesis of drug candidates targeting diseases like cancer, infections, or neurological disorders.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow solid |
| PURITY | 97-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿585.00 |
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| 1.000 | 10-20 days | ฿1,880.00 |
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| 5.000 | 10-20 days | ฿6,700.00 |
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Methyl (S)-4-Benzyl-5-oxomorpholine-3-carboxylate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the production of various bioactive molecules, including those with potential therapeutic applications. Its structural features make it valuable for constructing complex morpholine derivatives, which are often explored for their pharmacological properties, such as enzyme inhibition or receptor modulation. Additionally, it is employed in research settings to study stereochemistry and reaction mechanisms due to its chiral center. Its role in medicinal chemistry is significant, as it contributes to the synthesis of drug candidates targeting diseases like cancer, infections, or neurological disorders.
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