152915-90-7

Basic information

• Product Name: Pyrimidine, 5-bromo-2-[4-(phenylmethoxy)phenyl]-
• CAS NO: 152915-90-7
• Molecular Formula: C17H13BrN2O
• Molecular Weight: 341.207
• Mol File: 152915-90-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Pyrimidine, 5-bromo-2-[4-(phenylmethoxy)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimidine, 5-bromo-2-[4-(phenylmethoxy)phenyl]-(152915-90-7)
• EPA Substance Registry System: Pyrimidine, 5-bromo-2-[4-(phenylmethoxy)phenyl]-(152915-90-7)

Safety Data

• Hazardous Substances Data: 152915-90-7(Hazardous Substances Data)

Upstream product

• 603-35-0 triphenylphosphine 
• 32779-37-6 2,5-dibromopyrimidine 
• 146631-00-7 [4-(benzyloxy)phenyl]boronic acid 
• 7440-05-3 palladium 
• 7440-44-0 pyrographite 
• 183438-24-6 5-bromo-2-iodopyrimidine 
• 167018-88-4 2-(2',3'-difluoro-4'-octyloxyphenyl)-5-bromopyrimidine 
• 106-41-2 4-bromo-phenol 

Relevant articles and documents

Palladium-catalyzed Suzuki cross-coupling reactions in a microemulsion

An enhancement of palladium-catalyzed Suzuki cross-coupling reactions between substrates possessing long-chain alkyl or oxyalkyl substituents in two-phase media, in the presence of sodium dodecylsulfate, is shown. Quantitative evaluations of the influence of SDS on the reaction rates were determined.

Pyrimidine compounds

5-Bromo-2-iodopyrimidine is used to synthesize a range of chemical compounds including liquid crystalline compounds.

Process for cross-coupling aromatic boronic acids with aromatic halogen compounds or perfluoroalkylsulfonates

A process for preparing polycyclic aromatic compounds by cross-coupling aromatic boronic acids with aromatic halogen compounds or perfluoroalkylsulfonates in the presence of metallic palladium, if desired applied to a support material, as catalyst, wherei