C₂₂H₂₆O₆S

Base Information

Chemical Name:C₂₂H₂₆O₆S
CAS No.:1195988-27-2
Molecular Formula:C₂₂H₂₆O₆S
Molecular Weight:418.511
Hs Code.:

C<sub>22</sub>H<sub>26</sub>O<sub>6</sub>S

Synonyms:C₂₂H₂₆O₆S

Suppliers and Price of C₂₂H₂₆O₆S

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of C₂₂H₂₆O₆S

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of C₂₂H₂₆O₆S

There total 2 articles about C₂₂H₂₆O₆S 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: 98.0%

: 1195988-16-9
C₁₅H₂₀O₄

: 98-59-9
p-toluenesulfonyl chloride

: 1195988-27-2
C₂₂H₂₆O₆S

Guidance literature:: With di(n-butyl)tin oxide; triethylamine; In dichloromethane; at 20 ℃; for 14h;
DOI:10.1021/ol902217q

Reference yield:

: 1195988-14-7
C₂₃H₃₆O₄Si

: 1195988-27-2
C₂₂H₂₆O₆S

Guidance literature:: Multi-step reaction with 4 steps

1.1: diisobutylaluminium hydride / hexane; dichloromethane / 0.5 h / -78 - -50 °C

1.2: -78 - 20 °C

2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 13 h / 0 - 20 °C

3.1: titanium(IV) isopropylate; diethyl (2R,3R)-tartrate; Cumene hydroperoxide / dichloromethane / 9 h / -40 - -25 °C / Molecular sieve

3.2: 1.5 h / -25 - 20 °C

4.1: di(n-butyl)tin oxide; triethylamine / dichloromethane / 13.83 h / 20 °C

With titanium(IV) isopropylate; diethyl (2R,3R)-tartrate; Cumene hydroperoxide; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; di(n-butyl)tin oxide; triethylamine; In tetrahydrofuran; hexane; dichloromethane; 3.1: Sharpless epoxidation;
DOI:10.1016/j.tet.2010.11.017