(1,5-Cyclooctadiene)bis(methyldiphenylphosphine)iridium(I) (hexafluorophosphate)

(1,5-Cyclooctadiene)bis(methyldiphenylphosphine)iridium(I) (hexafluorophosphate)

• CAS Number: 38465-86-0
• UNSPSC Description: (1,5-Cyclooctadiene)bis(methyldiphenylphosphine)iridium(I) hexafluorophosphate is a highly efficient catalyst with excellent hydrogenation activity. It can catalyze the reaction of hydrogen and organic substrates in various chemical reactions. This compound is often used to synthesize important chemical intermediates and compounds.
• Target Antigen: Endogenous Metabolite
• Type: Reference compound
• Related Pathways: Metabolic Enzyme/Protease
• Assay Protocol: https://www.medchemexpress.com/1-5-cyclooctadiene-bis-methyldiphenylphosphine-iridium-i-hexafluorophosphate.html
• Smiles: C[Ir+](C)([P](C1=CC=CC=C1)(C)C2=CC=CC=C2)[P](C3=CC=CC=C3)(C)C4=CC=CC=C4.F[P-](F)(F)(F)(F)F.C5=C\CC/C=C\CC/5
• Molecular Weight: 845.79
• References & Citations: [1]Synthesis of Chiral Esters of (E)-3-(Silyloxy)-2-propenylboronic Acid via the Iridium-Catalyzed Isomerization of the Double Bond|[2]Isomerisation of allyl ethers catalysed by the cationic iridium complex [Ir (cyclo-octa-1, 5-diene)(PMePh 2) 2] PF 6|[3]Stereoselective Isomerization of Unsymmetrical Diallyl Ethers to Allyl (E)-Vinyl Ethers by a Cationic Iridium Catalyst|[4]Intramolecular allylboration of γ-(-formylalkoxy) allylboronates for syntheses of trans-or cis-2-(ethenyl) tetrahydropyran-3-ol and 2-(ethenyl) oxepan-3-ol
• Shipping Conditions: Room temperature
• Clinical Information: No Development Reported