(S)-()-3-Aminopiperidine dihydrochloride

98%

Reagent Code: #234220
label
Alias (S)-(+)-3-aminopiperidine dihydrochloride (S)-(+)-3-aminopiperidine
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CAS Number 334618-07-4

science Other reagents with same CAS 334618-07-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.08 g/mol
Formula C₅H₁₂N₂·₂HCl
badge Registry Numbers
MDL Number MFCD03427036
thermostat Physical Properties
Melting Point 190-195 °C
inventory_2 Storage & Handling
Storage Room temperature, avoid light

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its primary application lies in the production of central nervous system (CNS) agents, including antidepressants and antipsychotics, where the (S)-enantiomer contributes to desired biological activity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid piperidine scaffold and functional handles for derivatization. Also utilized in the preparation of enzyme inhibitors and receptor agonists/antagonists, especially targeting GPCRs and kinases. Suitable for solid-phase and solution-phase peptide-like synthesis in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿132.00
inventory 1g
10-20 days ฿380.00
inventory 5g
10-20 days ฿1,100.00
inventory 25g
10-20 days ฿4,780.00
inventory 100g
10-20 days ฿17,380.00
(S)-()-3-Aminopiperidine dihydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its primary application lies in the production of central nervous system (CNS) agents, including antidepressants and antipsychotics, where the (S)-enantiomer contributes to desired biological activity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid piperidine scaffold

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its primary application lies in the production of central nervous system (CNS) agents, including antidepressants and antipsychotics, where the (S)-enantiomer contributes to desired biological activity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its rigid piperidine scaffold and functional handles for derivatization. Also utilized in the preparation of enzyme inhibitors and receptor agonists/antagonists, especially targeting GPCRs and kinases. Suitable for solid-phase and solution-phase peptide-like synthesis in drug discovery.

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