(S)-2-(2-(methylthio)phenyl)pyrrolidine
95%
- Product Code: 123705
CAS:
1213556-30-9
| Molecular Weight: | 193.31 g./mol | Molecular Formula: | C₁₁H₁₅NS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08057893 | |
| Melting Point: | Boiling Point: | 283.0±33.0 °C(Predicted) | |
| Density: | 1.10±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
(S)-2-(2-(methylthio)phenyl)pyrrolidine finds application primarily in the field of medicinal chemistry and pharmaceutical research. It is utilized as a key intermediate or building block in the synthesis of various biologically active compounds. Its structure, featuring a pyrrolidine ring and a methylthio-phenyl group, makes it valuable for designing molecules with potential therapeutic properties. Researchers often explore its use in developing drugs targeting neurological disorders, such as depression or anxiety, due to its potential interaction with neurotransmitter systems. Additionally, it may serve as a precursor in the creation of ligands for receptor studies, aiding in the understanding of biochemical pathways and drug discovery processes. Its chiral nature also makes it useful in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿15,831.00 |
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| 0.250 | 10-20 days | ฿23,688.00 |
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(S)-2-(2-(methylthio)phenyl)pyrrolidine
(S)-2-(2-(methylthio)phenyl)pyrrolidine finds application primarily in the field of medicinal chemistry and pharmaceutical research. It is utilized as a key intermediate or building block in the synthesis of various biologically active compounds. Its structure, featuring a pyrrolidine ring and a methylthio-phenyl group, makes it valuable for designing molecules with potential therapeutic properties. Researchers often explore its use in developing drugs targeting neurological disorders, such as depression or anxiety, due to its potential interaction with neurotransmitter systems. Additionally, it may serve as a precursor in the creation of ligands for receptor studies, aiding in the understanding of biochemical pathways and drug discovery processes. Its chiral nature also makes it useful in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
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