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Home  > Adenosine,3'-[[(2S)-2-amino-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-N,N-dimethyl-, dihydrochloride

AI52978

58-58-2 | Adenosine,3'-[[(2S)-2-amino-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-N,N-dimethyl-, dihydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
1mg 98% in stock $25.00 $17.00 -   +
25mg 98% in stock $45.00 $32.00 -   +
50mg 98% in stock $63.00 $45.00 -   +
100mg 98% in stock $117.00 $82.00 -   +
500mg 98% in stock $540.00 $378.00 -   +

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Description
Catalog Number: AI52978
Chemical Name: Adenosine,3'-[[(2S)-2-amino-3-(4-methoxyphenyl)-1-oxopropyl]amino]-3'-deoxy-N,N-dimethyl-, dihydrochloride
CAS Number: 58-58-2
Molecular Formula: C22H31Cl2N7O5
Molecular Weight: 544.4314
MDL Number: MFCD00012691
SMILES: OC[C@H]1O[C@H]([C@@H]([C@@H]1NC(=O)[C@H](Cc1ccc(cc1)OC)N)O)n1cnc2c1ncnc2N(C)C.Cl.Cl

 

Computed Properties
Complexity: 680  
Covalently-Bonded Unit Count: 3  
Defined Atom Stereocenter Count: 5  
Heavy Atom Count: 36  
Hydrogen Bond Acceptor Count: 10  
Hydrogen Bond Donor Count: 6  
Rotatable Bond Count: 8  

 

 

Upstream Synthesis Route 
  • The application of (S)-2-Amino-N-((2S,3S,4R,5R)-5-(6-(dimethylamino)-9H-purin-9-yl)-4-hydroxy-2-(hydroxymethyl)tetrahydrofuran-3-yl)-3-(4-methoxyphenyl)propanamide dihydrochloride in chemical synthesis involves its utilization as a chiral building block or ligand in asymmetric transformations. This compound can serve as a key reagent for the selective formation of complex molecules with control over stereochemistry, making it a valuable tool in the synthesis of pharmaceuticals, natural products, and other fine chemicals. Its unique structural features and stereochemical properties enable it to act as a catalyst or intermediate in various synthetic pathways, facilitating the creation of intricate molecular architectures with high levels of stereoselectivity and purity.
Literature
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