C₃₅H₃₁NS₄

Base Information

Chemical Name:C₃₅H₃₁NS₄
CAS No.:1616787-12-2
Molecular Formula:C₃₅H₃₁NS₄
Molecular Weight:593.902
Hs Code.:

C<sub>35</sub>H<sub>31</sub>NS<sub>4</sub>

Synonyms:

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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 C₃₅H₃₁NS₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

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Technology Process of C₃₅H₃₁NS₄

There total 8 articles about C₃₅H₃₁NS₄ 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:

: 92289-14-0
3-(4-Nitro-phenyl)-pentanedioic acid

: 1616787-12-2
C₃₅H₃₁NS₄

Guidance literature:: Multi-step reaction with 6 steps

1: thionyl chloride / dichloromethane / 2 h / 20 °C

2: aluminum (III) chloride / dichloromethane / 20 °C

3: tin(ll) chloride; hydrogenchloride / ethanol; water / 80 °C

4: toluene-4-sulfonic acid / toluene / 110 °C / Dean-Stark

5: titanium trichloride tris(tetrahydrofuran); zinc / tetrahydrofuran / 1 h / 40 °C / Inert atmosphere

6: dichloromethane / UV-irradiation

With hydrogenchloride; aluminum (III) chloride; thionyl chloride; titanium trichloride tris(tetrahydrofuran); toluene-4-sulfonic acid; tin(ll) chloride; zinc; In tetrahydrofuran; ethanol; dichloromethane; water; toluene; 2: |Friedel-Crafts Acylation / 4: |Paal-Knorr Pyrrole Synthesis / 5: |McMurry Reaction;
DOI:10.1016/j.tet.2014.06.005

Reference yield:

: 1616787-08-6
3-(4-Nitro-phenyl)-pentanedioyl dichloride

: 1616787-12-2
C₃₅H₃₁NS₄

Guidance literature:: Multi-step reaction with 5 steps

1: aluminum (III) chloride / dichloromethane / 20 °C

2: tin(ll) chloride; hydrogenchloride / ethanol; water / 80 °C

3: toluene-4-sulfonic acid / toluene / 110 °C / Dean-Stark

4: titanium trichloride tris(tetrahydrofuran); zinc / tetrahydrofuran / 1 h / 40 °C / Inert atmosphere

5: dichloromethane / UV-irradiation

With hydrogenchloride; aluminum (III) chloride; titanium trichloride tris(tetrahydrofuran); toluene-4-sulfonic acid; tin(ll) chloride; zinc; In tetrahydrofuran; ethanol; dichloromethane; water; toluene; 1: |Friedel-Crafts Acylation / 3: |Paal-Knorr Pyrrole Synthesis / 4: |McMurry Reaction;
DOI:10.1016/j.tet.2014.06.005

Reference yield:

: 1616787-09-7
1,5-bis(2,5-dimethylthiophen-3-yl)-3-(4-nitrophenyl)pentane-1,5-dione

: 1616787-12-2
C₃₅H₃₁NS₄

Guidance literature:: Multi-step reaction with 4 steps

1: tin(ll) chloride; hydrogenchloride / ethanol; water / 80 °C

2: toluene-4-sulfonic acid / toluene / 110 °C / Dean-Stark

3: titanium trichloride tris(tetrahydrofuran); zinc / tetrahydrofuran / 1 h / 40 °C / Inert atmosphere

4: dichloromethane / UV-irradiation

With hydrogenchloride; titanium trichloride tris(tetrahydrofuran); toluene-4-sulfonic acid; tin(ll) chloride; zinc; In tetrahydrofuran; ethanol; dichloromethane; water; toluene; 2: |Paal-Knorr Pyrrole Synthesis / 3: |McMurry Reaction;
DOI:10.1016/j.tet.2014.06.005