C₃₅H₄₀N₂O₃S

Base Information

Chemical Name:C₃₅H₄₀N₂O₃S
CAS No.:959687-58-2
Molecular Formula:C₃₅H₄₀N₂O₃S
Molecular Weight:568.78
Hs Code.:

C<sub>35</sub>H<sub>40</sub>N<sub>2</sub>O<sub>3</sub>S

Synonyms:C₃₅H₄₀N₂O₃S

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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 C₃₅H₄₀N₂O₃S

Chemical Property:

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Technology Process of C₃₅H₄₀N₂O₃S

There total 11 articles about C₃₅H₄₀N₂O₃S 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:

: 943519-40-2
2,4-bisbenzyloxy-5-isopropyl-N-[4-methoxy-3-(methyl(propyl)amino)phenyl]benzamide

: 959687-58-2
C₃₅H₄₀N₂O₃S

Guidance literature:: With Lawessons reagent; In toluene; at 110 ℃; for 3h;

Reference yield:

: 100-44-7
benzyl chloride

: 959687-58-2
C₃₅H₄₀N₂O₃S

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 80 °C / Inert atmosphere

2: lithium hydroxide; water / methanol; tetrahydrofuran / 16 h / Heating

3: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 1 h / 20 °C / Cooling with ice

4: triethylamine / tetrahydrofuran / 16 h / 20 °C / Cooling with ice

5: Lawessons reagent / toluene / 3 h / 110 °C

With Lawessons reagent; oxalyl dichloride; water; potassium carbonate; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 943519-38-8
2,4-bisbenzyloxy-5-isopropylbenzoic acid methyl ester

: 959687-58-2
C₃₅H₄₀N₂O₃S

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hydroxide; water / methanol; tetrahydrofuran / 16 h / Heating

2: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 1 h / 20 °C / Cooling with ice

3: triethylamine / tetrahydrofuran / 16 h / 20 °C / Cooling with ice

4: Lawessons reagent / toluene / 3 h / 110 °C

With Lawessons reagent; oxalyl dichloride; water; triethylamine; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; toluene;