C₄₄H₃₀Cl₂O₄P₂Pt

Base Information

Chemical Name:C₄₄H₃₀Cl₂O₄P₂Pt
CAS No.:1598430-57-9
Molecular Formula:C₄₄H₃₀Cl₂O₄P₂Pt
Molecular Weight:950.653
Hs Code.:

C<sub>44</sub>H<sub>30</sub>Cl<sub>2</sub>O<sub>4</sub>P<sub>2</sub>Pt

Synonyms:

Suppliers and Price of C₄₄H₃₀Cl₂O₄P₂Pt

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

Total 0 raw suppliers

Chemical Property of C₄₄H₃₀Cl₂O₄P₂Pt

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₄H₃₀Cl₂O₄P₂Pt

There total 7 articles about C₄₄H₃₀Cl₂O₄P₂Pt 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:

: 18531-99-2
(S)-[1,1']-binaphthalenyl-2,2'-diol

: 1598430-57-9
C₄₄H₃₀Cl₂O₄P₂Pt

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine

2: triethylamine / diethyl ether; tetrahydrofuran / 20 h / 0 - 20 °C / Schlenk technique; Inert atmosphere

3: dichloromethane; acetonitrile / 16 h / 20 °C / Schlenk technique; Inert atmosphere

With triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; acetonitrile;
DOI:10.1002/ejic.201301255

Reference yield:

: 860519-27-3
1-bromo-2-(2-methoxyphenoxy)benzene

: 1598430-57-9
C₄₄H₃₀Cl₂O₄P₂Pt

Guidance literature:: Multi-step reaction with 4 steps

1.1: tert.-butyl lithium / hexane; tetrahydrofuran / 1 h / -78 °C / Schlenk technique; Inert atmosphere

1.2: 20 h / -78 - 20 °C / Schlenk technique; Inert atmosphere

2.1: boron tribromide; sodium hydrogencarbonate / dichloromethane; water / 20 h / -78 - 20 °C / Schlenk technique; Inert atmosphere

3.1: triethylamine / diethyl ether; tetrahydrofuran / 20 h / 0 - 20 °C / Schlenk technique; Inert atmosphere

4.1: dichloromethane; acetonitrile / 16 h / 20 °C / Schlenk technique; Inert atmosphere

With tert.-butyl lithium; boron tribromide; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; water; acetonitrile;
DOI:10.1002/ejic.201301255

Reference yield:

: 95-56-7
2-hydroxybromobenzene

: 1598430-57-9
C₄₄H₃₀Cl₂O₄P₂Pt

Guidance literature:: Multi-step reaction with 5 steps

1.1: 2,2,6,6-tetramethylheptane-3,5-dione; caesium carbonate; copper(l) chloride / 1-methyl-pyrrolidin-2-one / 120 °C / Schlenk technique; Inert atmosphere

2.1: tert.-butyl lithium / hexane; tetrahydrofuran / 1 h / -78 °C / Schlenk technique; Inert atmosphere

2.2: 20 h / -78 - 20 °C / Schlenk technique; Inert atmosphere

3.1: boron tribromide; sodium hydrogencarbonate / dichloromethane; water / 20 h / -78 - 20 °C / Schlenk technique; Inert atmosphere

4.1: triethylamine / diethyl ether; tetrahydrofuran / 20 h / 0 - 20 °C / Schlenk technique; Inert atmosphere

5.1: dichloromethane; acetonitrile / 16 h / 20 °C / Schlenk technique; Inert atmosphere

With 2,2,6,6-tetramethylheptane-3,5-dione; tert.-butyl lithium; boron tribromide; sodium hydrogencarbonate; caesium carbonate; triethylamine; copper(l) chloride; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; diethyl ether; hexane; dichloromethane; water; acetonitrile;
DOI:10.1002/ejic.201301255