(S)-Quinuclidin-3-ol

97%

  • Product Code: 37806
  CAS:    34583-34-1
Molecular Weight: 127.18 g./mol Molecular Formula: C₇H₁₃NO
EC Number: MDL Number:
Melting Point: Boiling Point: 206.9°C
Density: Storage Condition: 2-8°C
Product Description: (S)-Quinuclidin-3-ol is primarily used as a chiral building block in the synthesis of various pharmaceutical compounds. Its rigid bicyclic structure and stereochemistry make it valuable in the development of drugs targeting the central nervous system, particularly for neurological disorders. It serves as a key intermediate in the production of muscarinic receptor antagonists, which are used to treat conditions like overactive bladder and chronic obstructive pulmonary disease. Additionally, it is utilized in the preparation of ligands for nicotinic acetylcholine receptors, contributing to research in addiction and cognitive enhancement. Its versatility in asymmetric synthesis also makes it a valuable tool in medicinal chemistry for creating enantiomerically pure compounds.
Product Specification:
Test Specification
APPEARANCE White to Off-White Solid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿6,100.00
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0.250 10-20 days ฿18,160.00
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(S)-Quinuclidin-3-ol
(S)-Quinuclidin-3-ol is primarily used as a chiral building block in the synthesis of various pharmaceutical compounds. Its rigid bicyclic structure and stereochemistry make it valuable in the development of drugs targeting the central nervous system, particularly for neurological disorders. It serves as a key intermediate in the production of muscarinic receptor antagonists, which are used to treat conditions like overactive bladder and chronic obstructive pulmonary disease. Additionally, it is utilized in the preparation of ligands for nicotinic acetylcholine receptors, contributing to research in addiction and cognitive enhancement. Its versatility in asymmetric synthesis also makes it a valuable tool in medicinal chemistry for creating enantiomerically pure compounds.
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