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Home  > Inhibitors/Agonists  > Membrane Transporter/Ion Channel  > SGLT  > (2S,3R,4R,5S,6R)-2-[4-chloro-3-({4-[(3S)-oxolan-3-yloxy]phenyl}methyl)phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol

AB52385

864070-44-0 | (2S,3R,4R,5S,6R)-2-[4-chloro-3-({4-[(3S)-oxolan-3-yloxy]phenyl}methyl)phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $43.00 $30.00 -   +
1g 98% in stock $65.00 $45.00 -   +
5g 98% in stock $147.00 $103.00 -   +
10g 98% in stock $227.00 $159.00 -   +
25g 98% in stock $441.00 $309.00 -   +
100g 98% in stock $1,171.00 $820.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB52385
Chemical Name: (2S,3R,4R,5S,6R)-2-[4-chloro-3-({4-[(3S)-oxolan-3-yloxy]phenyl}methyl)phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol
CAS Number: 864070-44-0
Molecular Formula: C23H27ClO7
Molecular Weight: 450.9093
MDL Number: MFCD22566222
SMILES: OC[C@H]1O[C@@H](c2ccc(c(c2)Cc2ccc(cc2)O[C@@H]2COCC2)Cl)[C@@H]([C@H]([C@@H]1O)O)O

 

Computed Properties
Complexity: 558  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 6  
Heavy Atom Count: 31  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 4  
Rotatable Bond Count: 6  
XLogP3: 2  

 

 

Upstream Synthesis Route
  • The (1S)-1,5-Anhydro-1-C-[4-chloro-3-[[4-[[(3S)-tetrahydro-3-furanyl]oxy]phenyl]methyl]phenyl]-D-glucitol compound finds notable application in chemical synthesis processes where the strategic incorporation of specific regioselective functionalities is required. Its unique structure, featuring a chlorinated benzyl group attached to a furanose ring, offers a versatile platform for the construction of complex molecular architectures. (1S)-1,5-Anhydro-1-C-[4-chloro-3-[[4-[[(3S)-tetrahydro-3-furanyl]oxy]phenyl]methyl]phenyl]-D-glucitol serves as a valuable building block in the synthesis of biologically active compounds, pharmaceutical intermediates, and functional materials. Its ability to undergo selective transformations at different reactive sites enables chemists to access a diverse array of structurally diverse compounds with tailored properties and activities.
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