1-methanesulfonylpiperidin-3-aminehydrochloride

98%

Reagent Code: #213254
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CAS Number 1209712-99-1

science Other reagents with same CAS 1209712-99-1

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scatter_plot Molecular Information
Weight 214.71 g/mol
Formula C₆H₁₅ClN₂O₂S
badge Registry Numbers
MDL Number MFCD13196156
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules targeting central nervous system disorders. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs in drug discovery programs. Commonly employed in the preparation of kinase inhibitors and receptor modulators due to the amine group’s reactivity and the conformational stability provided by the piperidine ring. Also utilized in the production of sulfonamide-based compounds with potential anti-inflammatory and antimicrobial properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,990.00
inventory 250mg
10-20 days ฿14,450.00

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1-methanesulfonylpiperidin-3-aminehydrochloride
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules targeting central nervous system disorders. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs in drug discovery programs. Commonly employed in the preparation of kinase inhibitors and receptor modulators due to the amine group’s reactivity and the conformational stability provided by the piperidine ring. Als

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of biologically active molecules targeting central nervous system disorders. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs in drug discovery programs. Commonly employed in the preparation of kinase inhibitors and receptor modulators due to the amine group’s reactivity and the conformational stability provided by the piperidine ring. Also utilized in the production of sulfonamide-based compounds with potential anti-inflammatory and antimicrobial properties.

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