Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

5-(3-Thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide

Base Information Edit
  • Chemical Name:5-(3-Thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide
  • CAS No.:83101-59-1
  • Molecular Formula:C25H27N3O3S2
  • Molecular Weight:481.64
  • Hs Code.:
  • Mol file:83101-59-1.mol
5-(3-Thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide

Synonyms:5-(3-Thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide

Suppliers and Price of 5-(3-Thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide
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
Total 0 raw suppliers
Chemical Property of 5-(3-Thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 5-(3-Thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide

There total 7 articles about 5-(3-Thiocarbamoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide 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 TEA; hydrogen sulfide; In pyridine; Ambient temperature;
Guidance literature:
Multi-step reaction with 7 steps
1: 68 percent / NaBH4 / methanol
2: 85 percent / H2 / Raney-Ni / methanol / 760 Torr
3: 1.) HCl/NaNO2 / 1.) H2O; 2.) 0-5 deg C 30 min, room temp. 4 h
4: PBr3 / CHCl3 / 1.5 h / Heating
5: C2H2ONa / ethanol / 5 h / Heating
7: 97 percent / TEA, H2S / pyridine / Ambient temperature
With hydrogenchloride; sodium tetrahydroborate; C2H2ONa; TEA; hydrogen sulfide; hydrogen; phosphorus tribromide; sodium nitrite; nickel; In pyridine; methanol; ethanol; chloroform;
Guidance literature:
Multi-step reaction with 6 steps
1: 85 percent / H2 / Raney-Ni / methanol / 760 Torr
2: 1.) HCl/NaNO2 / 1.) H2O; 2.) 0-5 deg C 30 min, room temp. 4 h
3: PBr3 / CHCl3 / 1.5 h / Heating
4: C2H2ONa / ethanol / 5 h / Heating
6: 97 percent / TEA, H2S / pyridine / Ambient temperature
With hydrogenchloride; C2H2ONa; TEA; hydrogen sulfide; hydrogen; phosphorus tribromide; sodium nitrite; nickel; In pyridine; methanol; ethanol; chloroform;
Refernces Edit
Post RFQ for Price