(R)-2-Benzylmorpholine
95%
- Product Code: 55157
CAS:
131887-51-9
| Molecular Weight: | 177.2429 g./mol | Molecular Formula: | C₁₁H₁₅NO |
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| EC Number: | MDL Number: | MFCD14635495 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
(R)-2-Benzylmorpholine is widely utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its stereochemistry makes it particularly valuable in the development of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. The compound is often employed in the production of central nervous system (CNS) drugs, where precise stereochemical control is crucial for therapeutic activity. Additionally, it serves as an intermediate in the synthesis of analgesics and anti-inflammatory agents, contributing to the creation of more targeted and effective treatments. Its versatility also extends to the field of organic chemistry, where it is used in asymmetric synthesis and catalysis to produce complex molecules with high enantiomeric purity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,408.00 |
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(R)-2-Benzylmorpholine
(R)-2-Benzylmorpholine is widely utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its stereochemistry makes it particularly valuable in the development of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. The compound is often employed in the production of central nervous system (CNS) drugs, where precise stereochemical control is crucial for therapeutic activity. Additionally, it serves as an intermediate in the synthesis of analgesics and anti-inflammatory agents, contributing to the creation of more targeted and effective treatments. Its versatility also extends to the field of organic chemistry, where it is used in asymmetric synthesis and catalysis to produce complex molecules with high enantiomeric purity.
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