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N-BOC-3,4-Dihydro-2(1H)-quinolinone

Base Information
  • Chemical Name:N-BOC-3,4-Dihydro-2(1H)-quinolinone
  • CAS No.:194979-77-6
  • Molecular Formula:C14H17NO3
  • Molecular Weight:247.294
  • Hs Code.:2933790090
  • Mol file:194979-77-6.mol
N-BOC-3,4-Dihydro-2(1H)-quinolinone

Synonyms:

Suppliers and Price of N-BOC-3,4-Dihydro-2(1H)-quinolinone
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
  • N-Boc-3,4-Dihydro-2(1H)-quinolinone
  • 500mg
  • $ 175.00
  • Crysdot
  • N-BOC-3,4-Dihydro-2(1H)-quinolinone 95+%
  • 5g
  • $ 414.00
  • Chemenu
  • N-BOC-3,4-Dihydro-2(1H)-quinolinone 95%
  • 5g
  • $ 391.00
  • Alichem
  • N-BOC-3,4-Dihydro-2(1H)-quinolinone
  • 25g
  • $ 1232.20
  • Alichem
  • N-BOC-3,4-Dihydro-2(1H)-quinolinone
  • 5g
  • $ 407.00
  • AK Scientific
  • N-BOC-3,4-Dihydro-2(1H)-quinolinone
  • 1g
  • $ 184.00
Total 8 raw suppliers
Chemical Property of N-BOC-3,4-Dihydro-2(1H)-quinolinone
Chemical Property:
  • PSA:46.61000 
  • LogP:2.96590 
Purity/Quality:

99% *data from raw suppliers

N-Boc-3,4-Dihydro-2(1H)-quinolinone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses N-Boc-3,4-Dihydro-2(1H)-quinolinone is used for preparation of benzo[c]quinolizin-3-ones as potent and selective nonsteroidal inhibitors of human steroid 5α-reductase 1.
Technology Process of N-BOC-3,4-Dihydro-2(1H)-quinolinone

There total 6 articles about N-BOC-3,4-Dihydro-2(1H)-quinolinone 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 dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 6h; Inert atmosphere;
DOI:10.1039/c8cc03586e
Guidance literature:
With dmap; potassium hydrogensulfate; triethylamine; sodium chloride; In dichloromethane; water;
Guidance literature:
With Ir(CF3ppy)3; In acetonitrile; at 25 ℃; for 12h; Inert atmosphere; Irradiation;
DOI:10.1002/anie.202108775
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