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

(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.

Product Specifications

CAS Number

[38465-86-0]

UNSPSC

12352128

Hazard Statement

H302+H312+H332, H315, H319, H335

Target

Drug Intermediate; Endogenous Metabolite

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease; Others

Applications

Metabolism-protein/nucleotide metabolism

Assay Protocol

https://www.medchemexpress.com/1-5-cyclooctadiene-bis-methyldiphenylphosphine-iridium-i-hexafluorophosphate.html

Purity

97.0

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 Formula

C34H38IrP2.PF6

Molecular Weight

845.79

Precautions

H302+H312+H332, H315, H319, H335

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

Storage Conditions

4°C (Powder, protect from light, stored under nitrogen)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Available Sizes

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