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AI04841

10016-20-3 | a-Cyclodextrin

Packsize Purity Availability Price Discounted Price    Quantity
5g 95% in stock $13.00 $9.00 -   +
100g 95% in stock $39.00 $27.00 -   +

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Description
Catalog Number: AI04841
Chemical Name: a-Cyclodextrin
CAS Number: 10016-20-3
Molecular Formula: C36H60O30
Molecular Weight: 972.8436
MDL Number: MFCD00078207
SMILES: OC[C@H]1O[C@@H]2O[C@@H]3[C@@H](CO)O[C@@H]([C@@H](C3O)O)O[C@@H]3[C@@H](CO)O[C@@H]([C@@H]([C@H]3O)O)O[C@@H]3[C@H](O[C@H](O[C@@H]4[C@H](O[C@H](O[C@@H]5[C@H](O[C@H](O[C@H]1C([C@H]2O)O)[C@H](O)C5O)CO)[C@H](O)[C@@H]4O)CO)[C@@H]([C@@H]3O)O)CO

 

Computed Properties
Complexity: 1250  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 30  
Heavy Atom Count: 66  
Hydrogen Bond Acceptor Count: 30  
Hydrogen Bond Donor Count: 18  
Rotatable Bond Count: 6  
XLogP3: -12.9  

 

 

Upstream Synthesis Route 
  • $Name$ is a versatile compound that plays a crucial role in chemical synthesis, particularly in the realm of organic chemistry. Its unique molecular structure, consisting of a cyclic array of glucose units, allows $name$ to function as a complexing agent and chiral selector in various chemical reactions. In chemical synthesis, $name$ is extensively used for its ability to encapsulate guest molecules within its cavity. This inclusion complex formation not only enhances the solubility and stability of the guest molecules but also facilitates controlled release and targeted delivery in drug formulation and encapsulation processes. Furthermore, α-Cyclodextrin exhibits exceptional host-guest chemistry with a wide range of organic and inorganic compounds. Its selective molecular recognition properties enable it to selectively bind to specific guest molecules based on their size, shape, and polarity, thereby enabling the separation and purification of complex mixtures in organic synthesis.Additionally, in asymmetric synthesis, α-Cyclodextrin serves as a valuable chiral auxiliary or chiral inducer to promote enantioselective transformations and catalysis. By forming inclusion complexes with chiral substrates or catalysts, α-Cyclodextrin imparts chirality and stereochemical control to the reaction, leading to the formation of optically pure products with high enantiomeric excess.Overall, the application of α-Cyclodextrin in chemical synthesis encompasses a wide range of processes, from enhancing the reactivity and selectivity of reactions to enabling the efficient encapsulation and release of functional molecules. Its versatility and adaptability make it an indispensable tool for achieving tailored and precise outcomes in modern synthetic chemistry.
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