1318254-95-3

Basic information

• Product Name: 9-(4-bromophenyl)-2,6-dichloro-9H-purine
• Synonyms: 9-(4-bromophenyl)-2,6-dichloro-9H-purine
• CAS NO: 1318254-95-3
• Molecular Weight: 343.997
• Mol File: 1318254-95-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 9-(4-bromophenyl)-2,6-dichloro-9H-purine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(4-bromophenyl)-2,6-dichloro-9H-purine(1318254-95-3)
• EPA Substance Registry System: 9-(4-bromophenyl)-2,6-dichloro-9H-purine(1318254-95-3)

Safety Data

• Hazardous Substances Data: 1318254-95-3(Hazardous Substances Data)

Upstream product

• 589-87-7 1,4-bromoiodobenzene 
• 1228259-49-1 9,9,10,10,11,11,12,12,13,13,14,14,14-tridecafluoro-6-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)tetradec-1-yne 
• 114091-36-0 tributyl(trimethylgermyl)stannane 
• 65826-67-7 bis(4-bromophenyl)iodonium bromide 
• 5451-40-1 2,6 dichloropurine 

Relevant articles and documents

Extremely efficient and reversible visible-light photochromism and accompanying switch of electronic communication in N-phenylcarbazole-appended diethynylethene

Photoisomerization: N-phenylcarbazole-conjugated dimethyl 2,3-diethynylfumarate/maleate, E/Z-4, shows highly efficient and reversible visible-light E/Z photoisomerization (φtotal=0.40) upon excitation with an intramolecular charge-transfer band. This photochromism induces switching of electronic communication between the two N-phenylcarbazole moieties in the one-electron oxidized mixed-valent state (see scheme). Copyright

CuBr catalyzed C-N cross coupling reaction of purines and diaryliodonium salts to 9-arylpurines

CuBr was found to be an efficient catalyst for the C-N cross coupling reaction of purine and diaryliodonium salts. 9-Arylpurines were synthesized in excellent yields with short reaction times (2.5 h). The method represents an alternative to the synthesis of 9-arylpurines via Cu(ii) catalyzed C-N coupling reaction with arylboronic acids as arylating agents. The Royal Society of Chemistry 2011.