Reactant for: preparation of inhibitors of ataxia telangiectasia mutated and Rad3 related (ATR) protein kinase as potential anticancer agents, N-Methylation reactions of the pyridyl group, Palladium catalyzed amination reactions, intramolecular Heck reactions, Coupling reactions and Synthesis of trisubstituted pyrimidines from polyhalopyrimidines via Suzuki coupling.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Aplicaciones
Reactivo utilizado para la preparación de inhibidores de la ataxia telangiectasia mutada y proteína cinasa relacionada con la Rad3 (ATR) como potenciales agentes anticancerosos, reacciones de N-metilación del grupo piridil, reacciones de aminación catalizada de paladio, reacciones de Heck intramoleculares, reacciones de acoplamiento y síntesis de pirimidinas trisuki.
Solubilidad
Ligeramente soluble en agua.
Notas
Almacenar en un lugar fresco y seco en un recipiente cerrado herméticamente. Garantice una ventilación adecuada. Almacenar alejado de agentes oxidantes.
RUO – Research Use Only
General References:
- Minoru Ishikura; Tsukasa Ohta; Masanao Terashima. A Novel Synthesis of 4-Aryl-and 4-Heteroarylpyridines via Diethyl (4-pyridyl) borane. Chemical and Pharmaceutical Bulletin.1985 33(11), 4755-4763.
- Antonio Guarna; Ernesto G. Occhiato; Fabrizio Machetti; and Vittoria Giacomellia.19-Nor-10-azasteroids. 5.1 A Synthetic Strategy for the Preparation of (+)-17-(3-Pyridyl)-(5β)-10-azaestra-1,16- dien-3-one, a Novel Potential Inhibitor for Human Cytochrome P45017α (17α-Hydroxylase/C17,20-lyase). J. Org. Chem. 1999 64(13),4985-4989.