AC-11512 - 44-diiodobiphenyl-99 | 3001-15-8
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4,4'-Diiodobiphenyl
CAS:Formula:C12H8I2Purity:>98.0%(GC)Color and Shape:Light orange to Yellow to Green powder to crystalMolecular weight:406.004,4'-Diiodobiphenyl, 99%
CAS:<p>4,4?-diiodobiphenyl was coupled with (trimethylsilyl) acetylene via a Sonogashira-Hagihara reaction to afford the (trimethylsilyl)ethynyl derivative. 4,4?-diiodobipheny enhanced the expression of the luciferase gene. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesa</p>Formula:C12H8I2Purity:99%Color and Shape:Pale yellow, Crystals or powder or crystalline powderMolecular weight:406.014,4'-Diiodobiphenyl
CAS:4,4'-DiiodobiphenylPurity:98%Color and Shape:PowderMolecular weight:406.00g/mol4,4-Diiodobiphenyl
CAS:<p>4,4-Diiodobiphenyl is a synthetic organic compound that is created by the iodination reaction of biphenyl. The sodium hydrogen reacts with copper oxide in the presence of hydrochloric acid to create 4,4-diiodobiphenyl. This product can be used as a precursor to metal carbonyls and is therefore important in the chemical industry. 4,4-Diiodobiphenyl can also be used to synthesize other organic compounds, including diphenyl ethers. The environmental risks associated with this compound are its toxic properties and its ability to pollute water supplies.</p>Formula:C12H8I2Purity:Min. 95%Color and Shape:PowderMolecular weight:406 g/mol4,4′-Diiodobiphenyl
CAS:Formula:C12H8I2Purity:95%+Color and Shape:Solid, Beige powderMolecular weight:406.0054,4'-Diiodo-1,1'-biphenyl
CAS:Formula:C12H8I2Purity:95%Color and Shape:SolidMolecular weight:406.0009






