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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
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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