CAS Number | Molecular Formula | Molecular Weight | Density | Boiling Point |
---|---|---|---|---|
22276-95-5 | C6H3BrClN3 | 232.47 g/mol | 2.0±0.1 g/cm³ | 384.3°C |
Variant | CAS Number | Molecular Weight | Key Functional Groups |
---|---|---|---|
5-Bromo-4-chloro-7-methyl | 1266343-30-9 | 246.49 g/mol | Methyl substitution at 7-position |
4-Chloro-7H-pyrrolo(2,3-d)pyrimidine | 3680-69-1 | 153.57 g/mol | Absence of bromine substituent |
This compound serves as a critical precursor in synthesizing kinase inhibitors, particularly for oncology therapeutics. Its halogenated structure enables selective binding to ATP pockets in target enzymes.
Used in developing next-generation herbicides due to its stable heterocyclic framework, which enhances metabolic resistance in crop protection formulations.
For Suzuki coupling reactions: Use 1.2 eq Pd(PPh3)4 catalyst in degassed THF/H2O (3:1) at 80°C for 12 hours. Typical yields exceed 78%.
A Shanghai-based pharmaceutical company utilized this intermediate in synthesizing third-generation BTK inhibitors, achieving 92% purity after crystallization.
Beijing researchers incorporated derivatives into novel fungicides, demonstrating 98% efficacy against Puccinia striiformis in field trials.
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