4-((3-Hydroxypiperidin-1-yl)methyl)-N,N-dimethylbenzenesulfonamide

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Reagent Code: #196815
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CAS Number 1185320-06-2

science Other reagents with same CAS 1185320-06-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.401 g/mol
Formula C₁₄H₂₂N₂O₃S
badge Registry Numbers
MDL Number MFCD12195827
thermostat Physical Properties
Boiling Point 436.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.251 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of central nervous system agents. Shows potential in the design of receptor modulators due to its structural features that support blood-brain barrier penetration. Employed in research settings for optimizing compound libraries in drug discovery programs targeting neurological disorders. Its sulfonamide and hydroxyl functionalities allow for diverse chemical modifications, enhancing its utility in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿25,760.00

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4-((3-Hydroxypiperidin-1-yl)methyl)-N,N-dimethylbenzenesulfonamide
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of central nervous system agents. Shows potential in the design of receptor modulators due to its structural features that support blood-brain barrier penetration. Employed in research settings for optimizing compound libraries in drug discovery programs targeting neurological disorders. Its sulfonamide and hydroxyl functionalities allow for diverse chemical modifications, enhancing its utility in medicinal chemistry.

Used as an intermediate in pharmaceutical synthesis, particularly in the development of central nervous system agents. Shows potential in the design of receptor modulators due to its structural features that support blood-brain barrier penetration. Employed in research settings for optimizing compound libraries in drug discovery programs targeting neurological disorders. Its sulfonamide and hydroxyl functionalities allow for diverse chemical modifications, enhancing its utility in medicinal chemistry.

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