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trans-3-Hydroxy-6-methoxy-1-methyl-3,6-bis(phenylmethyl)-2,5-piperazinedione

Base Information
  • Chemical Name:trans-3-Hydroxy-6-methoxy-1-methyl-3,6-bis(phenylmethyl)-2,5-piperazinedione
  • CAS No.:87291-18-7
  • Molecular Formula:C20H22N2O4
  • Molecular Weight:354.406
  • Hs Code.:
  • Mol file:87291-18-7.mol
trans-3-Hydroxy-6-methoxy-1-methyl-3,6-bis(phenylmethyl)-2,5-piperazinedione

Synonyms:

Suppliers and Price of trans-3-Hydroxy-6-methoxy-1-methyl-3,6-bis(phenylmethyl)-2,5-piperazinedione
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 3 raw suppliers
Chemical Property of trans-3-Hydroxy-6-methoxy-1-methyl-3,6-bis(phenylmethyl)-2,5-piperazinedione
Chemical Property:
  • PSA:78.87000 
  • LogP:1.35800 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of trans-3-Hydroxy-6-methoxy-1-methyl-3,6-bis(phenylmethyl)-2,5-piperazinedione

There total 6 articles about trans-3-Hydroxy-6-methoxy-1-methyl-3,6-bis(phenylmethyl)-2,5-piperazinedione 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 hydrogen; triethylamine; palladium on activated charcoal; In ethyl acetate; for 0.5h; Ambient temperature;
DOI:10.1246/cl.1986.1453
Guidance literature:
Multi-step reaction with 6 steps
1: t-BuOK
3: 98 percent / t-BuOK
4: 95 percent / water, N-bromosuccinimide
5: 70 percent / N-bromosuccinimide / CHCl3 / 3 h / Ambient temperature
6: 60 percent / H2, triethylamine / 10 percent Pd/C / ethyl acetate / 0.5 h / Ambient temperature
With N-Bromosuccinimide; potassium tert-butylate; water; hydrogen; triethylamine; palladium on activated charcoal; In chloroform; ethyl acetate;
DOI:10.1246/cl.1986.1453
Guidance literature:
Multi-step reaction with 4 steps
1: 98 percent / t-BuOK
2: 95 percent / water, N-bromosuccinimide
3: 70 percent / N-bromosuccinimide / CHCl3 / 3 h / Ambient temperature
4: 60 percent / H2, triethylamine / 10 percent Pd/C / ethyl acetate / 0.5 h / Ambient temperature
With N-Bromosuccinimide; potassium tert-butylate; water; hydrogen; triethylamine; palladium on activated charcoal; In chloroform; ethyl acetate;
DOI:10.1246/cl.1986.1453
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