Indium, tris(phenylethynyl)-

Base Information

Chemical Name:Indium, tris(phenylethynyl)-
CAS No.:250643-76-6
Molecular Formula:C24H15In
Molecular Weight:418.203
Hs Code.:

Synonyms:

Suppliers and Price of Indium, tris(phenylethynyl)-

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

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Chemical Property of Indium, tris(phenylethynyl)-

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Indium, tris(phenylethynyl)-

There total 6 articles about Indium, tris(phenylethynyl)- 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:

: 6738-06-3
phenylethynylmagnesium bromide

: indium(III) chloride

: 250643-76-6
tris((2-phenyl)ethynyl)indium

Guidance literature:: In tetrahydrofuran; at -78 - 20 ℃; Inert atmosphere;
DOI:10.1016/j.jorganchem.2017.10.013

Reference yield:

: indium(III) chloride

: 536-74-3
phenylacetylene

: 250643-76-6
tris((2-phenyl)ethynyl)indium

Guidance literature:: indium(III) chloride; phenylacetylene; With n-butyllithium; at -78 - 20 ℃; Inert atmosphere;

indium(III) chloride; In tetrahydrofuran; at -78 - 20 ℃; Inert atmosphere;
DOI:10.1021/acs.orglett.6b02058

Reference yield:

: 10025-82-8
indium(III) chloride

: 4440-01-1
lithium phenylacetylide

: 250643-76-6
tris((2-phenyl)ethynyl)indium

Guidance literature:: In not given; under Ar; PhC2Li (3 equiv.) in THF or hexane or Et2O added slowly (15-30min) to cooled (-78°C) soln. of InCl3 in THF; stirred for 30 min ; warmed to room temp.; according to H. C. Clark, A. L. Pickard, J. Organomet. Chem. 8 (1967) 427;
DOI:10.1021/ja004195m