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

Encyclopedia

5-(4-Carbamimidoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide; hydriodide

Base Information Edit
  • Chemical Name:5-(4-Carbamimidoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide; hydriodide
  • CAS No.:83101-83-1
  • Molecular Formula:C25H28N4O3S*HI
  • Molecular Weight:592.501
  • Hs Code.:
  • Mol file:83101-83-1.mol
5-(4-Carbamimidoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide; hydriodide

Synonyms:

Suppliers and Price of 5-(4-Carbamimidoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide; hydriodide
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-(4-Carbamimidoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide; hydriodide Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 5-(4-Carbamimidoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide; hydriodide

There total 10 articles about 5-(4-Carbamimidoyl-phenyl)-2-(toluene-4-sulfonylamino)-pentanoic acid phenylamide; hydriodide 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 10 steps
1: 78 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
5: 1.) 6M HCl; 2.) 1M KOH / 1.) AcOH, reflux 3 h; 2.) Et2O, room temp. 2 h
6: SOCl2 / 1 h / Heating
7: 59 percent / benzene / 1.5 h / Ambient temperature
8: 72 percent / TEA, H2S / pyridine / Ambient temperature
9: 83.5 percent / acetone / Ambient temperature
10: 65 percent / 1.1M AcONH4 / ethanol / 2.5 h / Heating
With hydrogenchloride; potassium hydroxide; thionyl chloride; C2H2ONa; TEA; hydrogen sulfide; ammonium acetate; hydrogen; phosphorus tribromide; sodium nitrite; nickel; In pyridine; methanol; ethanol; chloroform; acetone; benzene;
Guidance literature:
Multi-step reaction with 11 steps
1: 70 percent / NaBH4 / methanol
2: 78 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
6: 1.) 6M HCl; 2.) 1M KOH / 1.) AcOH, reflux 3 h; 2.) Et2O, room temp. 2 h
7: SOCl2 / 1 h / Heating
8: 59 percent / benzene / 1.5 h / Ambient temperature
9: 72 percent / TEA, H2S / pyridine / Ambient temperature
10: 83.5 percent / acetone / Ambient temperature
11: 65 percent / 1.1M AcONH4 / ethanol / 2.5 h / Heating
With hydrogenchloride; potassium hydroxide; sodium tetrahydroborate; thionyl chloride; C2H2ONa; TEA; hydrogen sulfide; ammonium acetate; hydrogen; phosphorus tribromide; sodium nitrite; nickel; In pyridine; methanol; ethanol; chloroform; acetone; benzene;
Guidance literature:
Multi-step reaction with 7 steps
1: C2H2ONa / ethanol / 5 h / Heating
2: 1.) 6M HCl; 2.) 1M KOH / 1.) AcOH, reflux 3 h; 2.) Et2O, room temp. 2 h
3: SOCl2 / 1 h / Heating
4: 59 percent / benzene / 1.5 h / Ambient temperature
5: 72 percent / TEA, H2S / pyridine / Ambient temperature
6: 83.5 percent / acetone / Ambient temperature
7: 65 percent / 1.1M AcONH4 / ethanol / 2.5 h / Heating
With hydrogenchloride; potassium hydroxide; thionyl chloride; C2H2ONa; TEA; hydrogen sulfide; ammonium acetate; In pyridine; ethanol; acetone; benzene;
Post RFQ for Price