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Atomfair 5-Chloro-2,3-Diphenylpyrazine C16H11ClN2
Description 5-Chloro-2,3-Diphenylpyrazine (CAS No. 41270-66-0) is a high-purity heterocyclic organic compound with the molecular formula C16H11ClN2. This pyrazine derivative features a chloro-substituted ring system flanked by two phenyl groups, offering unique reactivity and structural versatility for synthetic applications. Our product is rigorously tested to ensure ??95% purity (HPLC) and is supplied as a crystalline solid with excellent batch-to-batch consistency. Ideal for pharmaceutical intermediates, materials science research, and coordination chemistry studies. Available in convenient packaging options from milligrams to kilogram quantities with full analytical documentation (COA, MSDS, NMR/HPLC data).
Description
Description
5-Chloro-2,3-Diphenylpyrazine (CAS No. 41270-66-0) is a high-purity heterocyclic organic compound with the molecular formula C16H11ClN2. This pyrazine derivative features a chloro-substituted ring system flanked by two phenyl groups, offering unique reactivity and structural versatility for synthetic applications. Our product is rigorously tested to ensure ??95% purity (HPLC) and is supplied as a crystalline solid with excellent batch-to-batch consistency. Ideal for pharmaceutical intermediates, materials science research, and coordination chemistry studies. Available in convenient packaging options from milligrams to kilogram quantities with full analytical documentation (COA, MSDS, NMR/HPLC data).
- CAS No: 41270-66-0
- Molecular Formula: C16H11ClN2
- Molecular Weight: 266.72
- Exact Mass: 266.0610761
- Monoisotopic Mass: 266.0610761
- IUPAC Name: 5-chloro-2,3-diphenylpyrazine
- SMILES: C1=CC=C(C=C1)C2=NC=C(N=C2C3=CC=CC=C3)Cl
- Synonyms: 5-chloro-2,3-diphenylpyrazine, 41270-66-0, DTXSID40394713, DTXCID90345573, 813-797-2
Application
5-Chloro-2,3-Diphenylpyrazine serves as a key building block in medicinal chemistry for developing kinase inhibitors and antimicrobial agents. The compound’s rigid aromatic structure makes it valuable in OLED material research as an electron-transport moiety. Researchers utilize its reactive chlorine substituent for palladium-catalyzed cross-coupling reactions in complex molecule synthesis.
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