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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > tert-Butyl 2-amino-5h-pyrrolo[3,4-d]pyrimidine-6(7h)-carboxylate

AD42926

1105187-42-5 | tert-Butyl 2-amino-5h-pyrrolo[3,4-d]pyrimidine-6(7h)-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $21.00 $15.00 -   +
1g 98% in stock $48.00 $34.00 -   +
5g 98% in stock $235.00 $165.00 -   +
25g 98% in stock $820.00 $574.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD42926
Chemical Name: tert-Butyl 2-amino-5h-pyrrolo[3,4-d]pyrimidine-6(7h)-carboxylate
CAS Number: 1105187-42-5
Molecular Formula: C11H16N4O2
Molecular Weight: 236.2703
MDL Number: MFCD08447404
SMILES: Nc1ncc2c(n1)CN(C2)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 302  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 0.1  

 

 

Upstream Synthesis Route
  • The application of tert-Butyl 2-amino-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate in chemical synthesis is significant due to its versatile reactivity and structural features. This compound serves as a valuable building block for the synthesis of various bioactive molecules and pharmaceutical compounds. It can undergo diverse chemical transformations, including functional group manipulations, cyclization reactions, and cross-coupling processes, enabling the construction of complex molecular frameworks with high efficiency. tert-Butyl 2-amino-5H-pyrrolo[3,4-d]pyrimidine-6(7H)-carboxylate plays a pivotal role in the development of novel drug candidates, agrochemicals, and materials by serving as a key intermediate in the synthesis of structurally diverse and pharmacologically relevant compounds. Its unique combination of heterocyclic motifs and functional groups makes it a valuable tool for chemists engaged in medicinal chemistry, organic synthesis, and chemical biology research.
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