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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > 4-Chloro-3,6-dimethylisoxazolo[5,4-d]pyrimidine

AI89442

1023758-00-0 | 4-Chloro-3,6-dimethylisoxazolo[5,4-d]pyrimidine

Packsize Purity Availability Price Discounted Price    Quantity
1mg 2 weeks $105.00 $73.00 -   +
2mg 2 weeks $123.00 $86.00 -   +
3mg 2 weeks $149.00 $105.00 -   +
5mg 2 weeks $168.00 $118.00 -   +
10mg 2 weeks $193.00 $135.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI89442
Chemical Name: 4-Chloro-3,6-dimethylisoxazolo[5,4-d]pyrimidine
CAS Number: 1023758-00-0
Molecular Formula: C7H6ClN3O
Molecular Weight: 183.5950
MDL Number: MFCD16992238
SMILES: Cc1nc(Cl)c2c(n1)onc2C

 

Computed Properties
Complexity: 180  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 4  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • 4-Chloro-3,6-dimethylisoxazolo[5,4-d]pyrimidine is a versatile chemical compound that finds significant application in chemical synthesis processes. Its unique structure and reactivity make it a valuable building block for the creation of various functional molecules.In chemical synthesis, this compound can serve as a key intermediate for the preparation of diverse organic compounds. Its presence in a reaction pathway can facilitate the formation of complex structures and functional groups through a series of carefully controlled transformations. The 4-Chloro-3,6-dimethylisoxazolo[5,4-d]pyrimidine moiety can undergo substitution, addition, or elimination reactions to introduce specific substituents or functional groups at precise positions within a molecular framework.Furthermore, the reactivity of 4-Chloro-3,6-dimethylisoxazolo[5,4-d]pyrimidine allows for its incorporation into a variety of scaffolds, leading to the synthesis of biologically active compounds, pharmaceutical agents, agrochemicals, and materials of interest. Its ability to participate in diverse chemical reactions broadens the scope of synthetic strategies available to chemists, enabling the efficient construction of complex molecular architectures.Overall, the strategic utilization of 4-Chloro-3,6-dimethylisoxazolo[5,4-d]pyrimidine in chemical synthesis offers a powerful tool for designing and accessing novel compounds with desired properties and functionalities. Its role as a versatile building block highlights its importance in the realm of synthetic organic chemistry.
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