1-(Methylsulfonyl)piperazine hydrochloride
97%
- Product Code: 114516
CAS:
161357-89-7
| Molecular Weight: | 200.69 g./mol | Molecular Formula: | C₅H₁₃ClN₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02018964 | |
| Melting Point: | 216-219°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Primarily utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structural features make it valuable in the development of potential therapeutic agents, particularly in the design of compounds targeting neurological disorders. The methylsulfonyl group enhances the molecule's ability to interact with specific biological targets, while the piperazine moiety contributes to its solubility and bioavailability. Researchers often employ it in the creation of novel drug candidates, focusing on its potential to modulate receptor activity or enzyme function. Additionally, its hydrochloride form ensures stability and ease of handling during experimental procedures.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿450.00 |
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| 1.000 | 10-20 days | ฿990.00 |
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| 5.000 | 10-20 days | ฿3,480.00 |
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1-(Methylsulfonyl)piperazine hydrochloride
Primarily utilized in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structural features make it valuable in the development of potential therapeutic agents, particularly in the design of compounds targeting neurological disorders. The methylsulfonyl group enhances the molecule's ability to interact with specific biological targets, while the piperazine moiety contributes to its solubility and bioavailability. Researchers often employ it in the creation of novel drug candidates, focusing on its potential to modulate receptor activity or enzyme function. Additionally, its hydrochloride form ensures stability and ease of handling during experimental procedures.
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