2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine
- CAS No.90213-66-4
- GradeIndustrial / Pharmaceutical
- Availability● In Stock
High-purity 2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine (CAS 90213-66-4), a key pharmaceutical intermediate for advanced kinase inhibitor syntheses.
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Product Overview
2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine is a high-value heterocyclic building block widely employed in the synthesis of targeted kinase inhibitors and other advanced pharmaceutical actives. With its rigid fused-ring architecture and two reactive chlorine sites, this compound serves as a versatile scaffold for selective nucleophilic substitution reactions, enabling efficient construction of complex drug molecules under controlled conditions.
Specifications
| Molecular Formula | C6H3Cl2N3 |
|---|---|
| Molecular Weight | 188.01 g/mol |
| Melting Point | 247–250°C |
| Density | 1.79 g/cm³ |
| Boiling Point | 312°C at 760 mmHg |
| Refractive Index | 1.805 |
| Appearance | White powder |
| Purity | ≥99% |
| Moisture Content | ≤0.2% |
| Total Impurities | ≤1% |
| Single Impurity | ≤0.1% |
Industrial Applications
This compound is primarily utilized as a critical intermediate in the multi-step synthesis of Janus kinase (JAK) inhibitors, including the active pharmaceutical ingredient (API) precursor to Tofacitinib citrate. Its dual chloro-substitution pattern allows for sequential functionalization, making it indispensable in medicinal chemistry campaigns focused on immunomodulatory and anti-inflammatory therapeutics.
- Enables regioselective derivatization for structure-activity relationship (SAR) studies
- Compatible with standard cross-coupling and displacement protocols
- Supplied in pharma-grade quality with full analytical documentation
Handling and Storage
Store in a tightly sealed container in a cool, dry environment away from direct sunlight, heat sources, and moisture. For industrial use only—handle in accordance with good manufacturing practices (GMP) and relevant chemical safety guidelines.
