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AE33584

1435-55-8 | Hydroquinidine

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $9.00 $6.00 -   +
5g 98% in stock $25.00 $17.00 -   +
10g 98% in stock $46.00 $32.00 -   +
25g 98% in stock $98.00 $68.00 -   +
100g 98% in stock $386.00 $270.00 -   +

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Description
Catalog Number: AE33584
Chemical Name: Hydroquinidine
CAS Number: 1435-55-8
Molecular Formula: C20H26N2O2
Molecular Weight: 326.4326
MDL Number: MFCD00135599
SMILES: CC[C@H]1CN2CC[C@H]1C[C@@H]2[C@H](c1ccnc2c1cc(OC)cc2)O

 

Computed Properties
Complexity: 432  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 4  
Heavy Atom Count: 24  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 4  
XLogP3: 3.1  

 

 

Upstream Synthesis Route 
  • Hydroquinidine, also known as 6'-Methoxy-α-methyl Quinine, is a chiral compound that finds extensive application in chemical synthesis as a chiral auxiliary and as a resolving agent for enantiomeric mixtures. In organic chemistry, Hydroquinidine is commonly used in asymmetric synthesis to control the stereochemistry of reactions. Its ability to form diastereomeric complexes with chiral compounds helps in the separation of enantiomers, enabling the isolation of pure chiral products.Additionally, Hydroquinidine displays catalytic properties in various reactions, enhancing the enantioselectivity of processes such as reductions, oxidations, and alkylations. It serves as a versatile tool in the design and synthesis of pharmaceuticals, agrochemicals, and other fine chemicals where chirality plays a crucial role in determining biological activity and properties.The utility of Hydroquinidine in chemical synthesis extends to the field of medicinal chemistry, where it is utilized in the development of novel drug candidates and pharmaceutical intermediates. Its role in the preparation of enantiomerically pure compounds contributes to the production of safer and more effective medications with reduced side effects.Overall, Hydroquinidine's significance in chemical synthesis lies in its ability to facilitate the asymmetric construction of complex molecules, enabling the production of optically pure substances with high efficiency and selectivity.
Literature
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