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Benz[f]imidazo[1,2-a]quinoxalin-3(11H)-one, 8-hydroxy-2-[(4-hydroxyphenyl)methyl]-12-(phenylmethyl)-

Base Information Edit
  • Chemical Name:Benz[f]imidazo[1,2-a]quinoxalin-3(11H)-one, 8-hydroxy-2-[(4-hydroxyphenyl)methyl]-12-(phenylmethyl)-
  • CAS No.:114496-03-6
  • Molecular Formula:C28H21 N3 O3
  • Molecular Weight:447.493
  • Hs Code.:
  • Mol file:114496-03-6.mol
Benz[f]imidazo[1,2-a]quinoxalin-3(11H)-one,  8-hydroxy-2-[(4-hydroxyphenyl)methyl]-12-(phenylmethyl)-

Synonyms:Benz[f]imidazo[1,2-a]quinoxalin-3(11H)-one, 8-hydroxy-2-[(4-hydroxyphenyl)methyl]-12-(phenylmethyl)-

Suppliers and Price of Benz[f]imidazo[1,2-a]quinoxalin-3(11H)-one, 8-hydroxy-2-[(4-hydroxyphenyl)methyl]-12-(phenylmethyl)-
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
  • Biosynth Carbosynth
  • Coelenterazine-v
  • 20 mg
  • $ 2300.00
  • Biosynth Carbosynth
  • Coelenterazine-v
  • 10 mg
  • $ 1250.00
  • Biosynth Carbosynth
  • Coelenterazine-v
  • 5 mg
  • $ 750.00
  • Biosynth Carbosynth
  • Coelenterazine-v
  • 2 mg
  • $ 450.00
  • Biosynth Carbosynth
  • Coelenterazine-v
  • 1 mg
  • $ 250.00
Total 1 raw suppliers
Chemical Property of Benz[f]imidazo[1,2-a]quinoxalin-3(11H)-one, 8-hydroxy-2-[(4-hydroxyphenyl)methyl]-12-(phenylmethyl)- Edit
Chemical Property:
  • PSA:90.62000 
  • LogP:4.92180 
Purity/Quality:

Coelenterazine-v *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of Benz[f]imidazo[1,2-a]quinoxalin-3(11H)-one, 8-hydroxy-2-[(4-hydroxyphenyl)methyl]-12-(phenylmethyl)-

There total 13 articles about Benz[f]imidazo[1,2-a]quinoxalin-3(11H)-one, 8-hydroxy-2-[(4-hydroxyphenyl)methyl]-12-(phenylmethyl)- 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 8 steps
1.1: potassium fluoride / bis(η3-allyl-μ-chloropalladium(II)); di‐tert‐butyl‐(1‐phenylindol‐2‐yl)phosphane / water; tetrahydrofuran / 14 h / 20 °C / Inert atmosphere
2.1: tetrabutyl-ammonium chloride / bis-triphenylphosphine-palladium(II) chloride / toluene / 1.5 h / Inert atmosphere; Reflux
3.1: n-butyllithium / hexane; tetrahydrofuran / 0.25 h / 0 °C / Inert atmosphere
3.2: 1.5 h / 0 - 20 °C / Inert atmosphere
4.1: pyridine / dmap / 1 h / 20 - 60 °C / Inert atmosphere
5.1: Hoveyda-Grubbs catalyst second generation / 1,2-dichloro-ethane / 17 h / 90 °C / Inert atmosphere
6.1: boron trifluoride / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere
7.1: methanol / 14 h / 65 °C
8.1: hydrogenchloride / ethanol; water / 0 - 80 °C / Inert atmosphere
With pyridine; hydrogenchloride; methanol; potassium fluoride; n-butyllithium; boron trifluoride; tetrabutyl-ammonium chloride; dmap; bis-triphenylphosphine-palladium(II) chloride; Hoveyda-Grubbs catalyst second generation; bis(η3-allyl-μ-chloropalladium(II)); di‐tert‐butyl‐(1‐phenylindol‐2‐yl)phosphane; In tetrahydrofuran; ethanol; hexane; dichloromethane; water; 1,2-dichloro-ethane; toluene; 1.1: Suzuki-Miyaura coupling / 2.1: Stille Coupling;
Guidance literature:
Multi-step reaction with 4 steps
1: Hoveyda-Grubbs catalyst second generation / 1,2-dichloro-ethane / 17 h / 90 °C / Inert atmosphere
2: boron trifluoride / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere
3: methanol / 14 h / 65 °C
4: hydrogenchloride / ethanol; water / 0 - 80 °C / Inert atmosphere
With hydrogenchloride; methanol; boron trifluoride; Hoveyda-Grubbs catalyst second generation; In ethanol; dichloromethane; water; 1,2-dichloro-ethane;
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