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1-Ethyl-2-benzimidazolinone

Base Information
  • Chemical Name:1-Ethyl-2-benzimidazolinone
  • CAS No.:10045-45-1
  • Molecular Formula:C9H10 N2 O
  • Molecular Weight:162.191
  • Hs Code.:2933990090
  • European Community (EC) Number:233-148-1
  • UNII:M82W79SS4W
  • DSSTox Substance ID:DTXSID70143296
  • Nikkaji Number:J241.245D
  • Wikidata:Q27077147
  • Pharos Ligand ID:34V2HZ3SKXVS
  • Metabolomics Workbench ID:67951
  • ChEMBL ID:CHEMBL452887
  • Mol file:10045-45-1.mol
1-Ethyl-2-benzimidazolinone

Synonyms:1-EBIO;1-ethyl-2-benzimidazolinone;1-ethyl-2-benzimidazolone

Suppliers and Price of 1-Ethyl-2-benzimidazolinone
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
  • 1-EBIO
  • 10mg
  • $ 325.00
  • TRC
  • 1-EBIO
  • 5mg
  • $ 45.00
  • TRC
  • 1-EBIO
  • 10mg
  • $ 85.00
  • Tocris
  • 1-EBIO ≥99%(HPLC)
  • 50
  • $ 357.00
  • Tocris
  • 1-EBIO ≥99%(HPLC)
  • 10
  • $ 85.00
  • Sigma-Aldrich
  • 1-EBIO ≥98% (HPLC)
  • 10mg
  • $ 83.70
  • Sigma-Aldrich
  • 1-EBIO ≥98% (HPLC)
  • 50mg
  • $ 339.00
  • Matrix Scientific
  • 1-Ethyl-1,3-dihydro-2H-benzimidazol-2-one
  • 5g
  • $ 555.00
  • Matrix Scientific
  • 1-Ethyl-1,3-dihydro-2H-benzimidazol-2-one
  • 500mg
  • $ 144.00
  • Matrix Scientific
  • 1-Ethyl-1,3-dihydro-2H-benzimidazol-2-one
  • 1g
  • $ 167.00
Total 30 raw suppliers
Chemical Property of 1-Ethyl-2-benzimidazolinone
Chemical Property:
  • Melting Point:118-120 °C(Solv: ethyl acetate (141-78-6)) 
  • PKA:12.29±0.30(Predicted) 
  • PSA:37.79000 
  • Density:1.161g/cm3 
  • LogP:1.34950 
  • Storage Temp.:Store at RT 
  • Solubility.:DMSO: ≥20mg/mL 
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:162.079312947
  • Heavy Atom Count:12
  • Complexity:193
Purity/Quality:

99%, *data from raw suppliers

1-EBIO *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn 
  • Statements: 22-36 
  • Safety Statements: 26 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCN1C2=CC=CC=C2NC1=O
  • Description 1-EBIO is an activator of Ca2+-sensitive K+ channels (EC50 = 490 μM in T84 human carcinoma cells).This action is sensitive to the neurotoxin charybdotoxin (Ki = 3.5 nM). In mouse colonic epithelia, 1-EBIO also activates cAMP-sensitive K+ channels, a response this is inhibited by 293B.In this type of epithelium, but not mouse nasal epithelia, 1-EBIO activates both types of channels, resulting in large Cl- secretory currents.It also activates the human intermediate conductance Ca2+-activated K+ channel (EC50 = 74 μM).1-EBIO is currently used to study the role of these types of K+ channels in diverse physiological functions.
  • Uses 1-EBIO stimulates Cl- secretion in secretory epithelia through direct activation of clacium potassium channels.1-EBIO was used to study the electrical activity modulated by Ca+2-activated K+ channels in rat central neurons. The effect of 1-EBIO on human intermediate conductance channels was studied.The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients
Technology Process of 1-Ethyl-2-benzimidazolinone

There total 20 articles about 1-Ethyl-2-benzimidazolinone 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; at 60 ℃; for 1h;
Guidance literature:
With hydrogenchloride; In 1,4-dioxane; methanol; for 18h;
DOI:10.1016/S0040-4039(03)01037-2
Guidance literature:
In formamide; at 130 ℃; for 0.333333h;
DOI:10.1021/je00032a042
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