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2-Guanidinobenzimidazole

Base Information
  • Chemical Name:2-Guanidinobenzimidazole
  • CAS No.:5418-95-1
  • Deprecated CAS:108940-88-1,111682-91-8,79454-77-6,111682-91-8,79454-77-6
  • Molecular Formula:C8H9N5
  • Molecular Weight:175.193
  • Hs Code.:2933990090
  • European Community (EC) Number:226-527-8
  • NSC Number:10548
  • UNII:FQ07TOI8GZ
  • DSSTox Substance ID:DTXSID6063858
  • Nikkaji Number:J217.997K
  • Wikidata:Q27105394
  • Metabolomics Workbench ID:67719
  • Mol file:5418-95-1.mol
2-Guanidinobenzimidazole

Synonyms:2-benzimidazolylguanidine;2-benzimidazolylguanidine dihydrochloride;2-guanidinebenzimidazole;2-guanidino-benzimidazole;benzimidazolyl-2-guanidine

Suppliers and Price of 2-Guanidinobenzimidazole
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
  • N-1H-Benzimidazol-2-ylguanidine
  • 500mg
  • $ 319.00
  • TRC
  • N-1H-Benzimidazol-2-ylguanidine
  • 2.5g
  • $ 120.00
  • SynQuest Laboratories
  • 2-Guanidinobenzimiazole
  • 5 g
  • $ 248.00
  • SynQuest Laboratories
  • 2-Guanidinobenzimiazole
  • 1 g
  • $ 77.00
  • Sigma-Aldrich
  • 2-Guanidinobenzimidazole 95%
  • 5g
  • $ 38.90
  • Matrix Scientific
  • N-1H-Benzimidazol-2-ylguanidine
  • 500mg
  • $ 315.00
  • Chemenu
  • N-1H-Benzimidazol-2-ylguanidine 95%
  • 10g
  • $ 422.00
  • American Custom Chemicals Corporation
  • N-1H-BENZIMIDAZOL-2-YLGUANIDINE HYDRATE 95.00%
  • 0.5G
  • $ 726.00
  • Alichem
  • 1-(1H-Benzo[d]imidazol-2-yl)guanidine
  • 10g
  • $ 478.06
  • AK Scientific
  • N-1H-Benzimidazol-2-ylguanidine
  • 5g
  • $ 91.00
Total 24 raw suppliers
Chemical Property of 2-Guanidinobenzimidazole
Chemical Property:
  • Appearance/Colour:BROWN-PURPLE FINE CRYSTALLINE POWDER 
  • Vapor Pressure:1.05E-08mmHg at 25°C 
  • Melting Point:242-244 °C 
  • Refractive Index:1.6900 (estimate) 
  • Boiling Point:461.6 °C at 760 mmHg 
  • PKA:13.67±0.30(Predicted) 
  • Flash Point:233 °C 
  • PSA:90.58000 
  • Density:1.56 g/cm3 
  • LogP:1.74130 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • Solubility.:Soluble in DMSO (up to 50 mg/ml) or in Water (up to 4 mg/ml with warming) 
  • XLogP3:0.1
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:175.08579531
  • Heavy Atom Count:13
  • Complexity:211
Purity/Quality:

99%, *data from raw suppliers

N-1H-Benzimidazol-2-ylguanidine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: S24/25:Avoid contact with skin and eyes.; 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)N=C(N)N
  • Description 2GBI (5418-95-1) is a selective and state-dependent blocker of voltage-gated proton channels (Hv1).1?2GBI blocks the channel by binding to the voltage-sensing domain from its intracellular side.2,3? Inhibition of Hv1 is a potentially new target of intervention in various pathophysiological processes including inflammatory, cancer, bone resorption and neurodegenerative disease.4
  • Uses N-1H-Benzimidazol-2-ylguanidine is used as a reagent in the synthesis of novel fused pyrimidines and imidazoles as potential analgesics.
Technology Process of 2-Guanidinobenzimidazole

There total 8 articles about 2-Guanidinobenzimidazole 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 hydrogenchloride; In water; for 1h; Heating;
DOI:10.1002/jhet.5570430115
Guidance literature:
With hydrogenchloride; In water; for 3h; Reflux;
DOI:10.21608/ejchem.2020.29618.2639
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