1H-Imidazole, 2,2',2''-phosphinidynetris[1-(phenylmethyl)-

Base Information

Chemical Name:1H-Imidazole, 2,2',2''-phosphinidynetris[1-(phenylmethyl)-
CAS No.:799248-20-7
Molecular Formula:C30H27N6P
Molecular Weight:502.558
Hs Code.:

Synonyms:

Suppliers and Price of 1H-Imidazole, 2,2',2''-phosphinidynetris[1-(phenylmethyl)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of 1H-Imidazole, 2,2',2''-phosphinidynetris[1-(phenylmethyl)-

Chemical Property:

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1H-Imidazole, 2,2',2''-phosphinidynetris[1-(phenylmethyl)-

There total 1 articles about 1H-Imidazole, 2,2',2''-phosphinidynetris[1-(phenylmethyl)- 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: 66.0%

: 4238-71-5
1-benzylimidazole

: 799248-20-7
tris(1-benzylimidazole-2-yl)phosphine

Guidance literature:: 1-benzylimidazole; With n-butyllithium; In diethyl ether; hexane; at -70 - -30 ℃; Inert atmosphere;

With phosphorus trichloride; In diethyl ether; hexane; at -90 - 20 ℃; Inert atmosphere;
DOI:10.1021/ic901562d

Reference yield: 43.0%

: 25749-29-5
(triphenylarsine)gold(I) chloride

: 799248-20-7
tris(1-benzylimidazole-2-yl)phosphine

: 1204521-62-9
(tris(1-benzylimidazole-2-yl)phosphine)AuCl

Guidance literature:: In dichloromethane; byproducts: Ph3As; (N2) to soln. ligand in CH2Cl2 at 0°C Au complex was added, stirred for 1 h; soln. was evapd. in vacuo, residue was treated with hexane, dissolved inCH2Cl2 and layered with hexane; elem. anal.;
DOI:10.1021/ic901562d