(2S)-2-(4-Chlorophenyl)piperidine hydrochloride

98%

Reagent Code: #236511
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CAS Number 1391375-27-1

science Other reagents with same CAS 1391375-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.15 g/mol
Formula C₁₁H₁₅Cl₂N
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MDL Number MFCD12910626
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting the central nervous system. Shows potential in the development of analgesics and psychiatric medications due to its structural similarity to known dopamine and sigma receptor ligands. Also employed in the study of structure-activity relationships for piperidine-based drugs, aiding optimization of selectivity and potency. Its chiral purity supports investigation of stereospecific effects in neuropharmacology.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,650.00
inventory 250mg
10-20 days ฿8,770.00
inventory 1g
10-20 days ฿34,200.00
(2S)-2-(4-Chlorophenyl)piperidine hydrochloride
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting the central nervous system. Shows potential in the development of analgesics and psychiatric medications due to its structural similarity to known dopamine and sigma receptor ligands. Also employed in the study of structure-activity relationships for piperidine-based drugs, aiding optimization of selectivity and potency. Its chiral purity supports investigation of stereospecific eff

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly those targeting the central nervous system. Shows potential in the development of analgesics and psychiatric medications due to its structural similarity to known dopamine and sigma receptor ligands. Also employed in the study of structure-activity relationships for piperidine-based drugs, aiding optimization of selectivity and potency. Its chiral purity supports investigation of stereospecific effects in neuropharmacology.

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