(S)-(-)-3-Aminoquinuclidine dihydrochloride

98%

Reagent Code: #113886
label
Alias (S)-(-)-3-Amino-1-azabicyclo[2.2.2]octane dihydrochloride
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CAS Number 119904-90-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.12 g/mol
Formula C₇H₁₄N₂₂HCl
badge Registry Numbers
MDL Number MFCD00191753
thermostat Physical Properties
Melting Point 260°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(S)-(-)-3-Aminoquinuclidine dihydrochloride is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral compounds. It serves as a key intermediate in the production of various drugs, especially those targeting the central nervous system. Its chiral nature makes it valuable in creating enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in the study of receptor binding and enzyme inhibition, aiding in the discovery of new treatments for neurological disorders. The compound's stability and reactivity also make it a useful reagent in organic synthesis, contributing to the development of novel chemical entities.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White powder or crystals
Purity (HPLC) 98-100
Purity (Titration with HClO4) 97.5-100
Infrared Spectrum Conforms to Structure
Solubility Colorless to faint yellow clear (25 mg/mL, H2O)
Specific Rotation [A]20/D (C=1, H2O) -26 to -22

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿390.00
inventory 5g
10-20 days ฿3,270.00
inventory 25g
10-20 days ฿15,990.00
inventory 1g
10-20 days ฿940.00
(S)-(-)-3-Aminoquinuclidine dihydrochloride
(S)-(-)-3-Aminoquinuclidine dihydrochloride is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral compounds. It serves as a key intermediate in the production of various drugs, especially those targeting the central nervous system. Its chiral nature makes it valuable in creating enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in the study of receptor binding and enzyme inhibition, aiding in the discovery of new treatments for neurological disorders. The compound's stability and reactivity also make it a useful reagent in organic synthesis, contributing to the development of novel chemical entities.
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