2-allyl-6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one
CAS 955368-90-8
![Molecular structure of 2-allyl-6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one](https://hantongchem.com/wp-content/themes/hantong/molecules/molecule-images/955368-90-8.png)
CAS · 955368-90-8
Product Overview
2-allyl-6-(Methylthio)-1H-pyrazolo[3,4-d]pyriMidin-3(2H)-one is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Appearance | yellow to orange solid |
|---|---|
| Identification | The sample NMR spectrum must match with the spectrum of standard. The retention time of the major peak in the chromatogram of sample corresponds to that in the chromatogram of standard preparation. |
| Purity (by HPLC) | 98% min |
| Single impurity (HPLC) | 0.5% max |
| M+2 impurity | 0.15% max |
| Water content | 1% max |
Applications
2-allyl-6-(Methylthio)-1H-pyrazolo[3,4-d]pyrimidin-3(2H)-one is primarily used in pharmaceutical and chemical research as a heterocyclic intermediate. It serves as a building block in the synthesis of bioactive molecules, including kinase inhibitors, antiviral compounds, and other therapeutic candidates. The pyrazolopyrimidinone core provides a privileged scaffold for designing compounds that target enzymes or receptors involved in cellular signaling pathways. It is also employed in medicinal chemistry studies to explore structure–activity relationships (SAR), optimize pharmacokinetic properties, and develop new drug candidates. Additionally, it is used in organic synthesis research to investigate heterocyclic chemistry, substitution reactions, and functionalization strategies for complex molecular scaffolds.
Benefits
2-allyl-6-(Methylthio)-1H-pyrazolo[3,4-d]pyrimidin-3(2H)-one offers several advantages in chemical and pharmaceutical applications. Its heterocyclic structure provides a rigid and bioactive scaffold suitable for receptor or enzyme binding, supporting the design of potent and selective drug candidates. The allyl and methylthio substituents allow for further chemical modification, enabling tailored functionalization and optimization of molecular properties. Its stability under standard laboratory conditions ensures reproducible handling and reliable synthetic outcomes. The compound's defined structure and reactivity facilitate multi-step synthesis and SAR studies, making it a versatile intermediate for drug discovery and advanced chemical research.
Conclusion
2-allyl-6-(Methylthio)-1H-pyrazolo[3,4-d]pyrimidin-3(2H)-one is a valuable heterocyclic intermediate with applications in pharmaceutical development and organic synthesis research. Its rigid pyrazolopyrimidinone scaffold, combined with reactive substituents, allows efficient design, modification, and optimization of bioactive molecules. Overall, the compound supports drug discovery, medicinal chemistry studies, and the synthesis of complex functional heterocycles.
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