(S)-(-)-3-Aminoquinuclidine dihydrochloride
98%
Reagent
Code: #113886
Alias
(S)-(-)-3-Amino-1-azabicyclo[2.2.2]octane dihydrochloride
CAS Number
119904-90-4
blur_circular Chemical Specifications
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Molecular Information
Weight
199.12 g/mol
Formula
C₇H₁₄N₂₂HCl
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Registry Numbers
MDL Number
MFCD00191753
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Physical Properties
Melting Point
260°C
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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 |
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(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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