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AI52250

546-43-0 | Alantolactone

Packsize Purity Availability Price Discounted Price    Quantity
5mg 95% in stock $44.00 $31.00 -   +
100mg 95% in stock $111.00 $78.00 -   +
250mg 95% in stock $182.00 $127.00 -   +
1g 95% in stock $462.00 $323.00 -   +

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Description
Catalog Number: AI52250
Chemical Name: Alantolactone
CAS Number: 546-43-0
Molecular Formula: C15H20O2
Molecular Weight: 232.3181
MDL Number: MFCD00274568
SMILES: C[C@H]1CCC[C@]2(C1=C[C@H]1[C@@H](C2)OC(=O)C1=C)C
NSC Number: 93131

 

Computed Properties
Complexity: 421  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 4  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 2  
XLogP3: 3.7  

 

 

Upstream Synthesis Route 
  • The compound (3aR,5S,8aR,9aR)-5,8a-Dimethyl-3-methylene-3,3a,6,7,8,8a,9,9a-octahydronaphtho[2,3-b]furan-2(5H)-one has significant utility in chemical synthesis as a versatile building block for the construction of complex organic molecules. Its unique structure and reactivity make it a valuable intermediate in various synthetic pathways.This compound can serve as a key starting material for the synthesis of diverse natural products, pharmaceuticals, and functional materials. Its structural features allow for modifications at multiple positions, enabling the introduction of various functional groups or stereochemical elements during synthetic transformations.In particular, (3aR,5S,8aR,9aR)-5,8a-Dimethyl-3-methylene-3,3a,6,7,8,8a,9,9a-octahydronaphtho[2,3-b]furan-2(5H)-one can participate in strategic bond-forming reactions such as cycloadditions, cross-coupling reactions, and functional group interconversions. This compound's involvement in these synthetic processes allows for the efficient construction of complex molecular frameworks with defined stereocenters and functionality.Overall, the application of (3aR,5S,8aR,9aR)-5,8a-Dimethyl-3-methylene-3,3a,6,7,8,8a,9,9a-octahydronaphtho[2,3-b]furan-2(5H)-one in chemical synthesis facilitates the access to structurally diverse and biologically relevant compounds through rational and efficient synthetic routes.
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