C₃₆H₃₈O₁₂S₂

Base Information

Chemical Name:C₃₆H₃₈O₁₂S₂
CAS No.:72536-42-6
Molecular Formula:C₃₆H₃₈O₁₂S₂
Molecular Weight:726.823
Hs Code.:

C<sub>36</sub>H<sub>38</sub>O<sub>12</sub>S<sub>2</sub>

Synonyms:

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Chemical Property of C₃₆H₃₈O₁₂S₂

Chemical Property:

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Technology Process of C₃₆H₃₈O₁₂S₂

There total 9 articles about C₃₆H₃₈O₁₂S₂ 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:

: 38209-42-6
threo-2,3-bis-(α-hydroxy-4-hydroxy-3-methoxybenzyl)butane-1,4-diol

: 72536-42-6
C₃₆H₃₈O₁₂S₂

Guidance literature:: Multi-step reaction with 7 steps

1: HCl / ethanol / high temperature vacuum distillation or heating with KHSO₄ at 200 deg C under vacuum

2: 66 percent / HCl(conc.) / 0.5 h / Heating

3: 15 mg / HCl / acetone / 1 h / Heating

4: 21 mg / chromium trioxide / pyridine / 4 h / Heating

5: 82 percent / diethyl ether / 24 h / Ambient temperature

6: 96 percent / di-isobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -68 °C

7: pyridine / 48 h / 0 °C

With pyridine; chromium(VI) oxide; hydrogenchloride; diisobutylaluminum hydride; In tetrahydrofuran; pyridine; diethyl ether; ethanol; hexane; acetone;

Reference yield:

: 72536-33-5,92216-42-7,139239-90-0
4,8-dihydroxypinoresinol

: 72536-42-6
C₃₆H₃₈O₁₂S₂

Guidance literature:: Multi-step reaction with 6 steps

1: 66 percent / HCl(conc.) / 0.5 h / Heating

2: 15 mg / HCl / acetone / 1 h / Heating

3: 21 mg / chromium trioxide / pyridine / 4 h / Heating

4: 82 percent / diethyl ether / 24 h / Ambient temperature

5: 96 percent / di-isobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -68 °C

6: pyridine / 48 h / 0 °C

With pyridine; chromium(VI) oxide; hydrogenchloride; diisobutylaluminum hydride; In tetrahydrofuran; pyridine; diethyl ether; hexane; acetone;

Reference yield:

: 63281-70-9,66428-04-4,66701-58-4
2,6-bis-(4-acetoxy-3-methoxyphenyl)-3,7-dioxabicyclo<3.3.0>octane-4,8-dione

: 72536-42-6
C₃₆H₃₈O₁₂S₂

Guidance literature:: Multi-step reaction with 8 steps

1: 51 percent / LiAlH₄ / tetrahydrofuran / 5 h / Heating

2: HCl / ethanol / high temperature vacuum distillation or heating with KHSO₄ at 200 deg C under vacuum

3: 66 percent / HCl(conc.) / 0.5 h / Heating

4: 15 mg / HCl / acetone / 1 h / Heating

5: 21 mg / chromium trioxide / pyridine / 4 h / Heating

6: 82 percent / diethyl ether / 24 h / Ambient temperature

7: 96 percent / di-isobutylaluminium hydride / tetrahydrofuran; hexane / 3 h / -68 °C

8: pyridine / 48 h / 0 °C

With pyridine; chromium(VI) oxide; hydrogenchloride; lithium aluminium tetrahydride; diisobutylaluminum hydride; In tetrahydrofuran; pyridine; diethyl ether; ethanol; hexane; acetone;