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AE08902

100594-13-6 | 2-Amino-4-iodo-6-methoxypyrimidine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $105.00 $74.00 -   +
1g 95% in stock $201.00 $141.00 -   +
5g 95% in stock $758.00 $531.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE08902
Chemical Name: 2-Amino-4-iodo-6-methoxypyrimidine
CAS Number: 100594-13-6
Molecular Formula: C5H6IN3O
Molecular Weight: 251.02511
MDL Number: MFCD09265491
SMILES: COc1cc(I)nc(n1)N

 

Computed Properties
Complexity: 113  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 0.8  

 

 

Upstream Synthesis Route
  • 2-Amino-4-iodo-6-methoxypyrimidine, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure allows it to be utilized in a wide range of reactions and transformations to generate complex organic molecules. In organic synthesis, $name$ can serve as a key intermediate in the preparation of various pharmaceutical compounds, agrochemicals, and materials. Its amino and methoxy functional groups provide sites for further modification, enabling the introduction of diverse substituents to tailor the properties of the final product.Additionally, the iodo substituent on the pyrimidine ring makes $name$ a valuable precursor for cross-coupling reactions, such as Suzuki-Miyaura or Heck coupling, leading to the formation of biaryl compounds or functionalized heterocycles. This versatility makes $name$ a valuable tool for medicinal chemists and synthetic organic chemists alike, facilitating the construction of structurally complex molecules with specific biological or physical properties.
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