(R)-3-(4-Methoxyphenyl)morpholine
90%
- Product Code: 56095
CAS:
1213977-38-8
| Molecular Weight: | 193.2423 g./mol | Molecular Formula: | C₁₁H₁₅NO₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
(R)-3-(4-Methoxyphenyl)morpholine is primarily utilized in pharmaceutical research and development as a chiral building block. Its enantiomeric purity makes it valuable in the synthesis of biologically active compounds, particularly in the creation of drugs targeting the central nervous system. The morpholine ring structure and methoxyphenyl group contribute to its potential in modulating receptor activity, making it a key intermediate in the production of selective serotonin reuptake inhibitors (SSRIs) and other neuroactive agents. Additionally, it is explored in the development of novel therapeutics for conditions like depression, anxiety, and neurodegenerative disorders due to its ability to influence neurotransmitter systems. Its application extends to medicinal chemistry, where it aids in optimizing drug efficacy and reducing side effects through stereochemical control.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £366.80 |
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(R)-3-(4-Methoxyphenyl)morpholine
(R)-3-(4-Methoxyphenyl)morpholine is primarily utilized in pharmaceutical research and development as a chiral building block. Its enantiomeric purity makes it valuable in the synthesis of biologically active compounds, particularly in the creation of drugs targeting the central nervous system. The morpholine ring structure and methoxyphenyl group contribute to its potential in modulating receptor activity, making it a key intermediate in the production of selective serotonin reuptake inhibitors (SSRIs) and other neuroactive agents. Additionally, it is explored in the development of novel therapeutics for conditions like depression, anxiety, and neurodegenerative disorders due to its ability to influence neurotransmitter systems. Its application extends to medicinal chemistry, where it aids in optimizing drug efficacy and reducing side effects through stereochemical control.
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