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Penicillin-V-sulfoxid-1'-tert-butylaminocarbonyl-2',2',2'-trichlorethylester

Base Information
  • Chemical Name:Penicillin-V-sulfoxid-1'-tert-butylaminocarbonyl-2',2',2'-trichlorethylester
  • CAS No.:65538-81-0
  • Molecular Formula:C23H28Cl3N3O7S
  • Molecular Weight:596.916
  • Hs Code.:
Penicillin-V-sulfoxid-1'-tert-butylaminocarbonyl-2',2',2'-trichlorethylester

Synonyms:Penicillin-V-sulfoxid-1'-tert-butylaminocarbonyl-2',2',2'-trichlorethylester

Suppliers and Price of Penicillin-V-sulfoxid-1'-tert-butylaminocarbonyl-2',2',2'-trichlorethylester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Penicillin-V-sulfoxid-1'-tert-butylaminocarbonyl-2',2',2'-trichlorethylester
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Technology Process of Penicillin-V-sulfoxid-1'-tert-butylaminocarbonyl-2',2',2'-trichlorethylester

There total 1 articles about Penicillin-V-sulfoxid-1'-tert-butylaminocarbonyl-2',2',2'-trichlorethylester 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 lithium cobalt(I)-phthalocyanine; phenol; In acetone; for 1h; Ambient temperature;
Guidance literature:
Multi-step reaction with 2 steps
1: 62 percent / lithium cobalt(I)-phthalocyanine-4,5 THF, phenol / acetone / 1 h / Ambient temperature
2: 58 percent / tetrahydrofuran; H2O / 2 h / Ambient temperature
With lithium cobalt(I)-phthalocyanine; phenol; In tetrahydrofuran; water; acetone;
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