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S3I-201.2096

Base Information
  • Chemical Name:S3I-201.2096
  • CAS No.:1251902-43-8
  • Molecular Formula:C36H36N4O6S
  • Molecular Weight:652.771
  • Hs Code.:
S<sub>3</sub>I-201.2096

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Chemical Property of S3I-201.2096
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Technology Process of S3I-201.2096

There total 12 articles about S3I-201.2096 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:
With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; at 20 ℃;
DOI:10.1002/cmdc.201100194
Guidance literature:
Multi-step reaction with 6 steps
1.1: potassium tert-butylate / N,N-dimethyl-formamide / 21 h / 0 - 20 °C / Inert atmosphere
2.1: acetic acid / methanol / 3 h / 45 °C / Molecular sieve; Inert atmosphere
2.2: 12 h / 20 °C / Inert atmosphere
3.1: dichlorotriphenylphosphorane / chloroform / 12 h / 60 °C / Inert atmosphere
4.1: lithium hydroxide monohydrate; water / tetrahydrofuran / 0.17 h / 20 °C / Inert atmosphere
5.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 16 h / 120 °C / Inert atmosphere
6.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 20 °C
With lithium hydroxide monohydrate; palladium 10% on activated carbon; potassium tert-butylate; water; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; dichlorotriphenylphosphorane; In tetrahydrofuran; methanol; chloroform; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1002/cmdc.201100194
Guidance literature:
Multi-step reaction with 8 steps
1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere
2.1: aluminum (III) chloride / dichloromethane / 1 h / 0 °C / Inert atmosphere
3.1: palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine / ethyl acetate / 2 h / 20 °C
4.1: acetic acid / methanol / 3 h / 45 °C / Molecular sieve; Inert atmosphere
4.2: 12 h / 20 °C / Inert atmosphere
5.1: dichlorotriphenylphosphorane / chloroform / 12 h / 60 °C / Inert atmosphere
6.1: lithium hydroxide monohydrate; water / tetrahydrofuran / 0.17 h / 20 °C / Inert atmosphere
7.1: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 16 h / 120 °C / Inert atmosphere
8.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 20 °C
With aluminum (III) chloride; lithium hydroxide monohydrate; palladium 10% on activated carbon; water; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; dichlorotriphenylphosphorane; In tetrahydrofuran; methanol; dichloromethane; chloroform; dimethyl sulfoxide; ethyl acetate; 2.1: Friedel Crafts acylation / 3.1: Rosenmund reduction;
DOI:10.1002/cmdc.201100194
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