<2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan

Base Information

Chemical Name:<2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan
CAS No.:87494-57-3
Molecular Formula:C₂₈H₅₆*C₉₂H₁₂₂O₈S₂
Molecular Weight:1812.86
Hs Code.:

<2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>-<Cyclooctacosan>-Rotaxan

Synonyms:<2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan

Suppliers and Price of <2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan

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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 <2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan

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Technology Process of <2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan

There total 1 articles about <2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan 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: 10.0%

: 297-24-5
cyclooctacosane

: 87494-56-2
1,20-Bis<4-<(11-triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan

: 87494-57-3
<2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan

Guidance literature:: With toluene-4-sulfonic acid; at 100 ℃; for 1h;

Reference yield: 50.0%

: 87494-58-4
13-bromotridec-1-yne

: 87494-57-3
<2>-<1,20-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>icosan>--Rotaxan

: 87508-92-7
<2>-<14,33-Bis<4-<11-(triphenylmethoxy)undecyloxy>phenylsulfonyl>-1,45-hexatetracontadiin>--Rotaxan

Guidance literature:: With hexane; lithium diisopropyl amide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; at -55 - -10 ℃; for 5h;