((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane

Base Information

Chemical Name:((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane
CAS No.:1550166-78-3
Molecular Formula:C₂₉H₄₄O₇Si
Molecular Weight:532.75
Hs Code.:

Synonyms:((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane

Suppliers and Price of ((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane

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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 ((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane

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Technology Process of ((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane

There total 1 articles about ((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane 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: 97.0%

: 70069-04-4
2-hydroxymethyl-18-crown-6

: 58479-61-1
tert-butylchlorodiphenylsilane

: 1550166-78-3
((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane

Guidance literature:: 2-hydroxymethyl-18-crown-6; With 1H-imidazole; In dichloromethane; for 0.166667h; Inert atmosphere; Cooling;

tert-butylchlorodiphenylsilane; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.jfluchem.2013.12.005

Reference yield:

: 1550166-78-3
((1,4,7,10,13,16-hexaoxacyclooctadecan-2-yl)methoxy)-(tert-butyl)diphenylsilane

: [¹⁸F]tert-butyldiphenylsilyl fluoride

Guidance literature:: With [¹⁸F]-potassium fluoride; potassium carbonate; [2.2.2]cryptande; In acetonitrile; at 20 ℃; Reagent/catalyst; Solvent; Inert atmosphere;
DOI:10.1016/j.jfluchem.2013.12.005