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Fenretinide Glucuronide MonosodiuM Salt

Base Information
  • Chemical Name:Fenretinide Glucuronide MonosodiuM Salt
  • CAS No.:76177-99-6
  • Molecular Formula:C32H40NO8*Na
  • Molecular Weight:589.661
  • Hs Code.:
Fenretinide Glucuronide MonosodiuM Salt

Synonyms:

Suppliers and Price of Fenretinide Glucuronide MonosodiuM Salt
Supply Marketing:
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
  • Usbiological
  • Fenretinide Glucuronide Monosodium Salt
  • 5mg
  • $ 460.00
  • TRC
  • FenretinideGlucuronideMonosodiumSalt
  • 50mg
  • $ 1320.00
  • TRC
  • FenretinideGlucuronideMonosodiumSalt
  • 5mg
  • $ 165.00
Total 3 raw suppliers
Chemical Property of Fenretinide Glucuronide MonosodiuM Salt
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Fenretinide Glucuronide Monosodium Salt *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Fenretinide Glucuronide Monosodium Salt, is the metabolite of Fenretinide (F250000), which is a synthetic retinoid deriverative, substances related to vitamin A. They are also shown to be used for the treatment of cancer, as well as in the treatment of cystic fibrosis, rheumatoid arthritis, acne, and psoriasis.
Technology Process of Fenretinide Glucuronide MonosodiuM Salt

There total 5 articles about Fenretinide Glucuronide MonosodiuM Salt 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 sodium hydroxide; sodium methylate; Yield given. Multistep reaction; 1.) methanol, room t., 18h; 2.) methanol, water, 4.5h, room t.;
DOI:10.1016/S0008-6215(00)84568-1
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) silver oxide
2: 1.) thionylchloride; 2.) pyridine / 1.) ether, from -10degC to room t. during 1.5 h; 2.) benzene, 65h, room t.
3: 1.) sodium methoxide; 2.) sodium hydroxide / 1.) methanol, room t., 18h; 2.) methanol, water, 4.5h, room t.
With pyridine; sodium hydroxide; thionyl chloride; sodium methylate; silver(l) oxide;
DOI:10.1016/S0008-6215(00)84568-1
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) thionylchloride; 2.) pyridine / 1.) ether, from -10degC to room t. during 1.5 h; 2.) benzene, 65h, room t.
2: 1.) sodium methoxide; 2.) sodium hydroxide / 1.) methanol, room t., 18h; 2.) methanol, water, 4.5h, room t.
With pyridine; sodium hydroxide; thionyl chloride; sodium methylate;
DOI:10.1016/S0008-6215(00)84568-1
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