(R)-1-Benzyl-5-methyl-1,4-diazepane
97%
- Product Code: 37391
CAS:
1620097-06-4
| Molecular Weight: | 204.31 g./mol | Molecular Formula: | C₁₃H₂₀N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29075976 | |
| Melting Point: | Boiling Point: | 296.1±28.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
(R)-1-Benzyl-5-methyl-1,4-diazepane is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting the central nervous system. Its structural framework is often incorporated into the design of potential therapeutic agents, such as receptor modulators or enzyme inhibitors, due to its ability to influence specific biochemical pathways. Researchers also explore its applications in the development of drugs for neurological disorders, including anxiety, depression, and cognitive impairments. Additionally, its chiral nature makes it valuable in studies focused on enantioselective synthesis and the optimization of drug efficacy and safety profiles.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $142.64 |
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| 5.000 | 10-20 days | $428.26 |
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| 10.000 | 10-20 days | $713.88 |
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(R)-1-Benzyl-5-methyl-1,4-diazepane
(R)-1-Benzyl-5-methyl-1,4-diazepane is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting the central nervous system. Its structural framework is often incorporated into the design of potential therapeutic agents, such as receptor modulators or enzyme inhibitors, due to its ability to influence specific biochemical pathways. Researchers also explore its applications in the development of drugs for neurological disorders, including anxiety, depression, and cognitive impairments. Additionally, its chiral nature makes it valuable in studies focused on enantioselective synthesis and the optimization of drug efficacy and safety profiles.
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