(η3-C6H3(OP(tert-butyl)2)2)IrHCl

Base Information

Chemical Name:(η3-C6H3(OP(tert-butyl)2)2)IrHCl
CAS No.:671789-61-0
Molecular Formula:C₂₂H₄₀ClIrO₂P₂
Molecular Weight:626.179
Hs Code.:

Synonyms:

Suppliers and Price of (η3-C6H3(OP(tert-butyl)2)2)IrHCl

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TCI Chemical
2,6-Bis(di-tert-butylphosphinoxy)phenylchlorohydroiridium(III) >98.0%(HPLC)
200mg
$ 184.00

Chem-Impex
2,6-Bis(di-tert-butylphosphinoxy)phenylchlorohydroiridium(III),98%(HPLC) 98%(HPLC)
200MG
$ 210.56

AK Scientific
2,6-Bis(di-tert-butylphosphinoxy)phenylchlorohydroiridium(III)
200mg
$ 309.00

Total 4 raw suppliers

Chemical Property of (η3-C6H3(OP(tert-butyl)2)2)IrHCl

Chemical Property:

Purity/Quality:

98%,99%, ^*data from raw suppliers

2,6-Bis(di-tert-butylphosphinoxy)phenylchlorohydroiridium(III) >98.0%(HPLC) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (η3-C6H3(OP(tert-butyl)2)2)IrHCl

There total 1 articles about (η3-C6H3(OP(tert-butyl)2)2)IrHCl which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

: 12112-67-3
bis(1,5-cyclooctadiene)diiridium(I) dichloride

: 338800-20-7
1,3-bis(di-tert-butylphosphinooxy)benzene

: 671789-61-0
(η3-C6H3(OP(tert-butyl)2)2)IrHCl

Guidance literature:: In toluene; Ar; addn. of toluene to Ar-filled flask contg. 0.5 equiv. of Ir complex and 1.1 equiv. of ligand, stirred at 150°C (oil bath) for 12 h; rapidly cooled to 30°C, evapd. under vac., residue extd. with pentane under ultrasound, filtration, solid washed with pentane, dried under high vac.; elem. anal.;
DOI:10.1021/ja0385235