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2-(1,3-benzodioxol-5-yl)quinoline-4-carbonyl chloride

Base Information Edit
  • Chemical Name:2-(1,3-benzodioxol-5-yl)quinoline-4-carbonyl chloride
  • CAS No.:1160264-91-4
  • Molecular Formula:C17H10ClNO3
  • Molecular Weight:311.724
  • Hs Code.:
  • Mol file:1160264-91-4.mol
2-(1,3-benzodioxol-5-yl)quinoline-4-carbonyl chloride

Synonyms:

Suppliers and Price of 2-(1,3-benzodioxol-5-yl)quinoline-4-carbonyl chloride
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
  • Matrix Scientific
  • 2-(1,3-Benzodioxol-5-yl)quinoline-4-carbonyl chloride
  • 500mg
  • $ 237.00
  • Crysdot
  • 2-(Benzo[d][1,3]dioxol-5-yl)quinoline-4-carbonylchloride 97%
  • 5g
  • $ 752.00
  • Chemenu
  • 2-(Benzo[d][1,3]dioxol-5-yl)quinoline-4-carbonylchloride 97%
  • 5g
  • $ 711.00
  • AK Scientific
  • 2-(1,3-Benzodioxol-5-YL)quinoline-4-carbonylchloride
  • 1g
  • $ 394.00
Total 1 raw suppliers
Chemical Property of 2-(1,3-benzodioxol-5-yl)quinoline-4-carbonyl chloride Edit
Chemical Property:
Purity/Quality:

98%min *data from raw suppliers

2-(1,3-Benzodioxol-5-yl)quinoline-4-carbonyl chloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-(1,3-benzodioxol-5-yl)quinoline-4-carbonyl chloride

There total 6 articles about 2-(1,3-benzodioxol-5-yl)quinoline-4-carbonyl chloride 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 thionyl chloride; In tetrahydrofuran; at 45 ℃; for 6.5h; Cooling with ice;
DOI:10.1016/j.bmc.2017.09.004
Guidance literature:
Multi-step reaction with 2 steps
1: potassium hydroxide / ethanol / 85 °C
2: thionyl chloride / tetrahydrofuran / 6.5 h / 45 °C / Cooling with ice
With thionyl chloride; potassium hydroxide; In tetrahydrofuran; ethanol; 1: |Pfitzinger Quinoline Synthesis;
DOI:10.1016/j.bmc.2017.09.004
Guidance literature:
Multi-step reaction with 4 steps
1: hydroxylamine hydrochloride; sodium sulfate; hydrogenchloride / water / 2 h / Heating
2: sulfuric acid / 60 - 90 °C
3: potassium hydroxide / ethanol / 85 °C
4: thionyl chloride / tetrahydrofuran / 6.5 h / 45 °C / Cooling with ice
With hydrogenchloride; thionyl chloride; sulfuric acid; hydroxylamine hydrochloride; sodium sulfate; potassium hydroxide; In tetrahydrofuran; ethanol; water; 2: |Sandmeyer Reaction / 3: |Pfitzinger Quinoline Synthesis;
DOI:10.1016/j.bmc.2017.09.004
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