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1-[3-[(4-BroMophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol

Base Information
  • Chemical Name:1-[3-[(4-BroMophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol
  • CAS No.:1350960-66-5
  • Molecular Formula:C19H18BrN3O3S
  • Molecular Weight:448.34
  • Hs Code.:
  • Mol file:1350960-66-5.mol
1-[3-[(4-BroMophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol

Synonyms:2-(4-hydroxypiperidin-1-yl)-3-(4-bromophenylsulfonyl)quinoxaline

Suppliers and Price of 1-[3-[(4-BroMophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol
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
  • TRC
  • 1-[3-[(4-Bromophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol
  • 100mg
  • $ 1470.00
  • Matrix Scientific
  • 1-(3-(4-Bromophenylsulfonyl)quinoxalin-2-yl)piperidin-4-ol 95%
  • 5g
  • $ 3256.00
  • Matrix Scientific
  • 1-(3-(4-Bromophenylsulfonyl)quinoxalin-2-yl)piperidin-4-ol 95%
  • 1g
  • $ 1018.00
Total 3 raw suppliers
Chemical Property of 1-[3-[(4-BroMophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol
Chemical Property:
  • Boiling Point:654.9±55.0 °C(Predicted) 
  • PKA:14.36±0.20(Predicted) 
  • Density:1.579±0.06 g/cm3(Predicted) 
Purity/Quality:

98% *data from raw suppliers

1-[3-[(4-Bromophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 1-[3-[(4-Bromophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol is a novel PI3Ka inhibitors which demonstrated excellent antitumor activities against five human cell lines.
Technology Process of 1-[3-[(4-BroMophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol

There total 3 articles about 1-[3-[(4-BroMophenyl)sulfonyl]-2-quinoxalinyl]-4-piperidinol 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:
In isopropyl alcohol; at 80 ℃; for 0.166667h; Microwave irradiation; Sealed vessel;
DOI:10.1016/j.bmc.2012.03.026
Guidance literature:
Multi-step reaction with 3 steps
1: hydrazine hydrate / water / 0 - 20 °C
2: ethanol / Reflux
3: isopropyl alcohol / 0.17 h / 80 °C / Microwave irradiation; Sealed vessel
With hydrazine hydrate; In ethanol; water; isopropyl alcohol;
DOI:10.1016/j.bmc.2012.03.026
Guidance literature:
Multi-step reaction with 2 steps
1: ethanol / Reflux
2: isopropyl alcohol / 0.17 h / 80 °C / Microwave irradiation; Sealed vessel
In ethanol; isopropyl alcohol;
DOI:10.1016/j.bmc.2012.03.026
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