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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

AA10546

1027511-41-6 | Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $17.00 $12.00 -   +
1g 98% in stock $50.00 $35.00 -   +
5g 98% in stock $170.00 $119.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA10546
Chemical Name: Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate
CAS Number: 1027511-41-6
Molecular Formula: C9H8BrN3O2
Molecular Weight: 270.0827
MDL Number: MFCD10574908
SMILES: CCOC(=O)c1cnn2c1ncc(c2)Br

 

Computed Properties
Complexity: 252  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 3  
XLogP3: 1.2  

 

 

Upstream Synthesis Route
  • Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate is a versatile and valuable compound in chemical synthesis, particularly in the field of medicinal chemistry and drug discovery. Its unique structure makes it a key building block for the synthesis of complex molecules with potential pharmacological activities.In organic synthesis, Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate serves as a crucial intermediate in the preparation of biologically active compounds, including pharmaceuticals and agrochemicals. Its strategic placement of functional groups allows for further derivatization to introduce diverse substituents, enhancing the compound's potency and specificity in various biological assays.Researchers utilize Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate as a starting material to access novel chemical entities through efficient synthetic routes. By incorporating this compound into synthetic schemes, chemists can access a wide range of chemical space, enabling the discovery of new molecules with potential therapeutic applications.Overall, Ethyl 6-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate plays a pivotal role in chemical synthesis by offering a valuable platform for the development of biologically active compounds with diverse pharmacological properties. Its strategic utilization in synthetic pathways contributes to the advancement of medicinal chemistry research and drug development efforts.
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