C₃₆H₅₀O₂S₂

Base Information

Chemical Name:C₃₆H₅₀O₂S₂
CAS No.:1346260-31-8
Molecular Formula:C₃₆H₅₀O₂S₂
Molecular Weight:578.924
Hs Code.:

C<sub>36</sub>H<sub>50</sub>O<sub>2</sub>S<sub>2</sub>

Synonyms:C₃₆H₅₀O₂S₂

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Chemical Property of C₃₆H₅₀O₂S₂

Chemical Property:

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Technology Process of C₃₆H₅₀O₂S₂

There total 8 articles about C₃₆H₅₀O₂S₂ 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: 76.0%

: 1346260-30-7
C₁₀H₁₃BrS

: 74026-61-2
geranylgeranyl phenylsulfone

: 1346260-31-8
C₃₆H₅₀O₂S₂

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at -40 ℃; for 0.5h;

Reference yield:

: 498-62-4
3-thiophene carboxaldehyde

: 1346260-31-8
C₃₆H₅₀O₂S₂

Guidance literature:: Multi-step reaction with 8 steps

1: dichloromethane / 2 h / 20 °C

2: diisobutylaluminium hydride / dichloromethane / 0.5 h / 0 °C

3: palladium on activated charcoal; hydrogen / 4 h / 20 °C

4: pyridinium chlorochromate / dichloromethane / 10 h / 20 °C

5: dichloromethane / 0.5 h / 20 °C

6: diisobutylaluminium hydride / dichloromethane / 0.33 h / 0 °C

7: triphenylphosphine; carbon tetrabromide / 0.25 h / 0 °C

8: potassium tert-butylate / tetrahydrofuran / 0.5 h / -40 °C

With carbon tetrabromide; palladium on activated charcoal; potassium tert-butylate; hydrogen; diisobutylaluminium hydride; triphenylphosphine; pyridinium chlorochromate; In tetrahydrofuran; dichloromethane;

Reference yield:

: 50266-60-9
ethyl (2E)-3-(3-thienyl)propenoate

: 1346260-31-8
C₃₆H₅₀O₂S₂

Guidance literature:: Multi-step reaction with 7 steps

1: diisobutylaluminium hydride / dichloromethane / 0.5 h / 0 °C

2: palladium on activated charcoal; hydrogen / 4 h / 20 °C

3: pyridinium chlorochromate / dichloromethane / 10 h / 20 °C

4: dichloromethane / 0.5 h / 20 °C

5: diisobutylaluminium hydride / dichloromethane / 0.33 h / 0 °C

6: triphenylphosphine; carbon tetrabromide / 0.25 h / 0 °C

7: potassium tert-butylate / tetrahydrofuran / 0.5 h / -40 °C

With carbon tetrabromide; palladium on activated charcoal; potassium tert-butylate; hydrogen; diisobutylaluminium hydride; triphenylphosphine; pyridinium chlorochromate; In tetrahydrofuran; dichloromethane;