1-(Methylsulfonyl)piperazine hydrochloride
97%
Reagent
Code: #114516
CAS Number
161357-89-7
blur_circular Chemical Specifications
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Molecular Information
Weight
200.69 g/mol
Formula
C₅H₁₃ClN₂O₂S
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Registry Numbers
MDL Number
MFCD02018964
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Physical Properties
Melting Point
216-219°C
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Storage & Handling
Storage
room temperature, dry
description 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.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | White To Off-White Solid |
Purity (%) | 96.5-100% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
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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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