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1,3-Benzenedicarboxylic acid, 2,2'-thiobis[5-(1,1-dimethylethyl)-, tetraethyl ester

Base Information
  • Chemical Name:1,3-Benzenedicarboxylic acid, 2,2'-thiobis[5-(1,1-dimethylethyl)-, tetraethyl ester
  • CAS No.:62558-15-0
  • Molecular Formula:C32H42O8S
  • Molecular Weight:586.747
  • Hs Code.:
1,3-Benzenedicarboxylic acid, 2,2'-thiobis[5-(1,1-dimethylethyl)-,
tetraethyl ester

Synonyms:

Suppliers and Price of 1,3-Benzenedicarboxylic acid, 2,2'-thiobis[5-(1,1-dimethylethyl)-, tetraethyl ester
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Chemical Property of 1,3-Benzenedicarboxylic acid, 2,2'-thiobis[5-(1,1-dimethylethyl)-, tetraethyl ester
Chemical Property:
Purity/Quality:
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SDS file from LookChem

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Technology Process of 1,3-Benzenedicarboxylic acid, 2,2'-thiobis[5-(1,1-dimethylethyl)-, tetraethyl ester

There total 5 articles about 1,3-Benzenedicarboxylic acid, 2,2'-thiobis[5-(1,1-dimethylethyl)-, tetraethyl ester 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:
Guidance literature:
Multi-step reaction with 3 steps
1: 70 percent / NaOH, copper-bronze powder / dimethylformamide / 14 h / Heating
2: SOCl2 / Heating
3: pyridine / 1 h / Heating
With pyridine; sodium hydroxide; thionyl chloride; copper; In N,N-dimethyl-formamide;
DOI:10.1021/ja00391a023
Guidance literature:
Multi-step reaction with 3 steps
1: 70 percent / NaOH, copper-bronze powder / dimethylformamide / 14 h / Heating
2: SOCl2 / Heating
3: pyridine / 1 h / Heating
With pyridine; sodium hydroxide; thionyl chloride; copper; In N,N-dimethyl-formamide;
DOI:10.1021/ja00391a023
Guidance literature:
Multi-step reaction with 2 steps
1: SOCl2 / Heating
2: pyridine / 1 h / Heating
With pyridine; thionyl chloride;
DOI:10.1021/ja00391a023
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