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Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE

Base Information Edit
  • Chemical Name:Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE
  • CAS No.:114014-15-2
  • Molecular Formula:C31H34N4O5
  • Molecular Weight:542.635
  • Hs Code.:
  • Mol file:114014-15-2.mol
Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE

Synonyms:

Suppliers and Price of Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • DC Chemicals
  • CathepsinLinhibitorIII >98%
  • 250 mg
  • $ 1200.00
  • Cayman Chemical
  • Z-Phe-Tyr(tBu)-diazomethylketone
  • 25mg
  • $ 488.00
  • Cayman Chemical
  • Z-Phe-Tyr(tBu)-diazomethylketone
  • 10mg
  • $ 210.00
  • Cayman Chemical
  • Z-Phe-Tyr(tBu)-diazomethylketone
  • 5mg
  • $ 113.00
  • Cayman Chemical
  • Z-Phe-Tyr(tBu)-diazomethylketone
  • 1mg
  • $ 30.00
  • Biorbyt Ltd
  • Cathepsin L inhibitor III >98%
  • 1 g
  • $ 3136.50
  • Biorbyt Ltd
  • Cathepsin L inhibitor III >98%
  • 250 mg
  • $ 1802.00
  • Biorbyt Ltd
  • Cathepsin L inhibitor III >98%
  • 100 mg
  • $ 1060.80
Total 24 raw suppliers
Chemical Property of Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE Edit
Chemical Property:
  • Storage Temp.:-15°C 
Purity/Quality:

99%+, *data from raw suppliers

CathepsinLinhibitorIII >98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE

There total 4 articles about Z-PHE-TYR(TBU)-DIAZOMETHYLKETONE 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
2: N-methylmorpholine / 0.25 h / 0 °C
3: diethyl ether / 0 - 20 °C
With 4-methyl-morpholine; In diethyl ether; 2: Acylation / 3: Substitution;
DOI:10.1016/S0960-894X(00)00340-1
Guidance literature:
Multi-step reaction with 3 steps
2: N-methylmorpholine / 0.25 h / 0 °C
3: diethyl ether / 0 - 20 °C
With 4-methyl-morpholine; In diethyl ether; 2: Acylation / 3: Substitution;
DOI:10.1016/S0960-894X(00)00340-1
Guidance literature:
Multi-step reaction with 2 steps
1: N-methylmorpholine / 0.25 h / 0 °C
2: diethyl ether / 0 - 20 °C
With 4-methyl-morpholine; In diethyl ether; 1: Acylation / 2: Substitution;
DOI:10.1016/S0960-894X(00)00340-1
Refernces Edit
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