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Home  > 2-[(acetyloxy)methyl]-4-(2-amino-9H-purin-9-yl)butyl acetate

AB74206

104227-87-4 | 2-[(acetyloxy)methyl]-4-(2-amino-9H-purin-9-yl)butyl acetate

Packsize Purity Availability Price Discounted Price    Quantity
50mg 97% in stock $15.00 $10.00 -   +
100mg 97% in stock $18.00 $12.00 -   +
1g 97% in stock $23.00 $16.00 -   +
5g 97% in stock $55.00 $38.00 -   +
25g 97% in stock $163.00 $114.00 -   +
100g 97% in stock $449.00 $315.00 -   +

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Description
Catalog Number: AB74206
Chemical Name: 2-[(acetyloxy)methyl]-4-(2-amino-9H-purin-9-yl)butyl acetate
CAS Number: 104227-87-4
Molecular Formula: C14H19N5O4
Molecular Weight: 321.3317600000001
MDL Number: MFCD00866964
SMILES: CC(=O)OCC(CCn1cnc2c1nc(N)nc2)COC(=O)C
NSC Number: 758921

 

Computed Properties
Complexity: 404  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 23  
Hydrogen Bond Acceptor Count: 8  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 9  

 

 

Upstream Synthesis Route 
  • 2-[(Acetyloxy)methyl]-4-(2-amino-9H-purin-9-yl)butyl acetate is a versatile compound widely used in chemical synthesis. One key application lies in its role as a protecting group in peptide chemistry. By selectively acetylating the amino group of purine, this compound effectively masks the reactivity of the amine functionality. This protection strategy ensures that unwanted side reactions are minimized during subsequent synthetic steps, allowing for efficient and controlled assembly of peptide chains. Additionally, the acetyl group can be easily removed under mild conditions, revealing the free amine for further functionalization. This compound's ability to offer protection to specific functional groups makes it an invaluable tool in the synthesis of complex molecules and bioactive compounds.
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