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Glycine hydrobromide

Base Information
  • Chemical Name:Glycine hydrobromide
  • CAS No.:17219-65-7
  • Molecular Formula:C2H5NO2.BrH
  • Molecular Weight:155.979
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00600867
Glycine hydrobromide

Synonyms:2-Aminoacetic acid hydrobromide;17219-65-7;GLYCINE HYDROBROMIDE;SCHEMBL2325590;DTXSID00600867;Glycine--hydrogen bromide (1/1)

Suppliers and Price of Glycine hydrobromide
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 1 raw suppliers
Chemical Property of Glycine hydrobromide
Chemical Property:
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:154.95819
  • Heavy Atom Count:6
  • Complexity:42.9
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C(C(=O)O)N.Br
Technology Process of Glycine hydrobromide

There total 1 articles about Glycine hydrobromide 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 formate buffer; at 25 ℃; Rate constant; Product distribution; Mechanism; pH dependence, various conditions;
DOI:10.1002/jps.2600700812
Guidance literature:
In tetrahydrofuran; for 24h; Ambient temperature;
Guidance literature:
With Staphylococcus aureus V8 proteinase; triethylamine; In water; acetonitrile; at 30 ℃; for 24h;
DOI:10.1016/S0040-4039(00)92725-4
Downstream raw materials:

Z-(S)-Glu-Gly

Boc-L-Pro-ΔZ-Phe-Gly-NH2

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