4-(4-Chloro-phenylsulfanyl)-piperidinehydrochloride

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Reagent Code: #164338
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CAS Number 101798-64-5

science Other reagents with same CAS 101798-64-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.215 g/mol
Formula C₁₁H₁₅Cl₂NS
badge Registry Numbers
MDL Number MFCD03840148
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of centrally acting agents, particularly those targeting neurological pathways. Its structure supports development of compounds with potential antidepressant, anxiolytic, or cognitive-enhancing effects. The chloro-phenylsulfanyl moiety enhances blood-brain barrier penetration, making it valuable in designing neuroactive drugs. Also employed in structure-activity relationship (SAR) studies to optimize receptor binding, especially for serotonin and dopamine receptors. Limited use outside research due to lack of approved therapeutic products containing this exact scaffold.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿22,840.00

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4-(4-Chloro-phenylsulfanyl)-piperidinehydrochloride
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Used in pharmaceutical research as a key intermediate in the synthesis of centrally acting agents, particularly those targeting neurological pathways. Its structure supports development of compounds with potential antidepressant, anxiolytic, or cognitive-enhancing effects. The chloro-phenylsulfanyl moiety enhances blood-brain barrier penetration, making it valuable in designing neuroactive drugs. Also employed in structure-activity relationship (SAR) studies to optimize receptor binding, especially for sero
Used in pharmaceutical research as a key intermediate in the synthesis of centrally acting agents, particularly those targeting neurological pathways. Its structure supports development of compounds with potential antidepressant, anxiolytic, or cognitive-enhancing effects. The chloro-phenylsulfanyl moiety enhances blood-brain barrier penetration, making it valuable in designing neuroactive drugs. Also employed in structure-activity relationship (SAR) studies to optimize receptor binding, especially for serotonin and dopamine receptors. Limited use outside research due to lack of approved therapeutic products containing this exact scaffold.
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