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2-morpholino-8-(naphthalen-1-yl)-4H-1,3-benzoxazin-4-one

Base Information Edit
  • Chemical Name:2-morpholino-8-(naphthalen-1-yl)-4H-1,3-benzoxazin-4-one
  • CAS No.:1879887-94-1
  • Molecular Formula:C22H18N2O3
  • Molecular Weight:358.397
  • Hs Code.:
  • Mol file:1879887-94-1.mol
2-morpholino-8-(naphthalen-1-yl)-4H-1,3-benzoxazin-4-one

Synonyms:

Suppliers and Price of 2-morpholino-8-(naphthalen-1-yl)-4H-1,3-benzoxazin-4-one
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
  • TRC
  • LTURM36
  • 2.5mg
  • $ 225.00
  • Tocris
  • LTURM36 ≥98%(HPLC)
  • 50
  • $ 605.00
  • Tocris
  • LTURM36 ≥98%(HPLC)
  • 10
  • $ 144.00
Total 1 raw suppliers
Chemical Property of 2-morpholino-8-(naphthalen-1-yl)-4H-1,3-benzoxazin-4-one Edit
Chemical Property:
Purity/Quality:

≥98% by HPLC *data from raw suppliers

LTURM36 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses LTURM 36 is a specific DNA-PK inhibitor.
Technology Process of 2-morpholino-8-(naphthalen-1-yl)-4H-1,3-benzoxazin-4-one

There total 6 articles about 2-morpholino-8-(naphthalen-1-yl)-4H-1,3-benzoxazin-4-one 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 bis-triphenylphosphine-palladium(II) chloride; potassium carbonate; In 1,4-dioxane; water; at 50 ℃; for 16h; Schlenk technique; Inert atmosphere;
DOI:10.1016/j.ejmech.2016.01.042
Guidance literature:
Multi-step reaction with 4 steps
1.1: dichloromethane
2.1: sodium hydrogencarbonate / isopropyl alcohol; water / 60 °C
2.2: 0.5 h / 20 °C
3.1: isopropyl alcohol; water / 3 h / 20 °C
4.1: potassium carbonate; bis-triphenylphosphine-palladium(II) chloride / water; 1,4-dioxane / 16 h / 50 °C / Schlenk technique; Inert atmosphere
With bis-triphenylphosphine-palladium(II) chloride; sodium hydrogencarbonate; potassium carbonate; In 1,4-dioxane; dichloromethane; water; isopropyl alcohol;
DOI:10.1016/j.ejmech.2016.01.042
Guidance literature:
Multi-step reaction with 6 steps
1.1: bromine / water
2.1: sulfuric acid / water / 0.5 h / 20 - 172 °C / Microwave irradiation
3.1: dichloromethane
4.1: sodium hydrogencarbonate / isopropyl alcohol; water / 60 °C
4.2: 0.5 h / 20 °C
5.1: isopropyl alcohol; water / 3 h / 20 °C
6.1: potassium carbonate; bis-triphenylphosphine-palladium(II) chloride / water; 1,4-dioxane / 16 h / 50 °C / Schlenk technique; Inert atmosphere
With bis-triphenylphosphine-palladium(II) chloride; sulfuric acid; bromine; sodium hydrogencarbonate; potassium carbonate; In 1,4-dioxane; dichloromethane; water; isopropyl alcohol;
DOI:10.1016/j.ejmech.2016.01.042
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