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H-Gly-Pro-Arg-OH

Base Information
  • Chemical Name:H-Gly-Pro-Arg-OH
  • CAS No.:47295-77-2
  • Molecular Formula:C13H24N6O4
  • Molecular Weight:328.371
  • Hs Code.:
  • Mol file:47295-77-2.mol
H-Gly-Pro-Arg-OH

Synonyms:L-Arginine,N2-(1-glycyl-L-prolyl)-; 10: PN: EP1422237 SEQID: 10 unclaimed protein; 11: PN:WO2007015107 SEQID: 14 claimed protein; 17: PN: WO0004941 PAGE: 31 claimedprotein; 23: PN: KR20090132815 PAGE: 3 claimed sequence; 23: PN: KR20090132911SEQID: 118 claimed protein; 25: PN: WO2004069875 PAGE: 69 claimed protein; 2:PN: WO0102437 PAGE: 11 claimed protein; 324: PN: WO03026591 SEQID: 331unclaimed protein; Glycyl-L-prolyl-L-arginine

Suppliers and Price of H-Gly-Pro-Arg-OH
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
Total 11 raw suppliers
Chemical Property of H-Gly-Pro-Arg-OH
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:178.12000 
  • Density:1.54g/cm3 
  • LogP:0.43820 
Purity/Quality:

>98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of H-Gly-Pro-Arg-OH

There total 10 articles about H-Gly-Pro-Arg-OH 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 2 steps
1: hydrogenchloride / diethyl ether; ethyl acetate / 16 h
2: sodium chloride / 37 °C / aq. buffer
With hydrogenchloride; sodium chloride; In diethyl ether; ethyl acetate;
DOI:10.1039/b906762k
Guidance literature:
Multi-step reaction with 3 steps
1: dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0 - 20 °C
2: hydrogenchloride / diethyl ether; ethyl acetate / 16 h
3: sodium chloride / 37 °C / aq. buffer
With hydrogenchloride; dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium chloride; In diethyl ether; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1039/b906762k
Guidance literature:
Multi-step reaction with 5 steps
1: pyridine; trichlorophosphate / -15 - 20 °C
2: hydrogenchloride / diethyl ether; ethyl acetate / 20 °C
3: dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0 - 20 °C
4: hydrogenchloride / diethyl ether; ethyl acetate / 16 h
5: sodium chloride / 37 °C / aq. buffer
With pyridine; hydrogenchloride; dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium chloride; trichlorophosphate; In diethyl ether; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1039/b906762k
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