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Home  > (3E,4S)-3-{2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decahydronaphthalen-1-yl]ethylidene}-4-hydroxyoxolan-2-one

AB70735

5508-58-7 | (3E,4S)-3-{2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decahydronaphthalen-1-yl]ethylidene}-4-hydroxyoxolan-2-one

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $16.00 $11.00 -   +
1g 98% in stock $25.00 $17.00 -   +
5g 98% in stock $47.00 $33.00 -   +
25g 98% in stock $119.00 $83.00 -   +
100g 98% in stock $326.00 $228.00 -   +
250g 98% in stock $755.00 $528.00 -   +
500g 98% in stock $1,132.00 $793.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

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Description
Catalog Number: AB70735
Chemical Name: (3E,4S)-3-{2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-decahydronaphthalen-1-yl]ethylidene}-4-hydroxyoxolan-2-one
CAS Number: 5508-58-7
Molecular Formula: C20H30O5
Molecular Weight: 350.4492
MDL Number: MFCD07778082
SMILES: OC[C@]1(C)[C@H](O)CC[C@@]2([C@@H]1CCC(=C)[C@H]2C/C=C/1[C@H](O)COC1=O)C

 

Computed Properties
Complexity: 597  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 6  
Defined Bond Stereocenter Count: 1  
Heavy Atom Count: 25  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 3  
XLogP3: 2.2  

 

 

Upstream Synthesis Route 
  • (3E,4S)-3-[2-[(1R,4aS,5R,6R,8aS)-Decahydro-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylene-1-naphthalenyl]ethylidene]dihydro-4-hydroxy-2(3H)-furanone can be utilized as a chiral building block in chemical synthesis. Its unique structure containing both a furanone ring and a complex polycyclic system makes it a valuable intermediate for the creation of structurally diverse compounds. In synthesis, this compound can serve as a key precursor for the generation of bioactive molecules, pharmaceuticals, or natural product derivatives. Its chirality and functional groups offer opportunities for selective transformations and the construction of complex molecular architectures with specific stereochemical arrangements. This compound's presence in a synthetic route can enable the efficient assembly of intricate organic molecules with desired properties and functionalities.
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