Parameter | 4-Hydrazino-6-methylpyrimidin-2-amine | Analogous Pyrimidine Derivatives |
---|---|---|
CAS Number | N/A (Custom Synthesis) | Varies by compound |
Molecular Formula | C5H9N5 | C5H7N3 (e.g., 4-Amino-6-methylpyrimidine) |
Purity | >98% (HPLC) | 90-95% (Typical commercial grades) |
Storage Conditions | 2-8°C in inert atmosphere | Room temperature (non-hydrazino derivatives) |
Used in synthesis of kinase inhibitors targeting EGFR and VEGFR pathways. Enables functionalization at N2 position for enhanced bioavailability.
Key precursor for systemic fungicides with methylpyrimidine cores. Provides hydrazine handle for conjugation with triazole groups.
Acts as polydentate ligand for transition metal catalysts in cross-coupling reactions (e.g., Suzuki-Miyaura).
Optimized multi-step synthesis achieving 76% yield in c-Met inhibitor precursor production under GMP conditions.
Enabled 40% reduction in synthetic steps for broad-spectrum fungicide registration in EU markets.
Accelerated lead optimization phase by 5 months through reliable supply of GLP-grade material for IND-enabling studies.
Scaled production to metric ton quantities for novel strobilurin-class fungicide with 99.2% batch consistency.
Contact our technical team for batch-specific COAs and custom synthesis options:
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