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1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride

Base Information Edit
  • Chemical Name:1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride
  • CAS No.:1233955-50-4
  • Molecular Formula:C12H16BrN3O*ClH
  • Molecular Weight:334.643
  • Hs Code.:
  • Mol file:1233955-50-4.mol
1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride

Synonyms:

Suppliers and Price of 1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride
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
  • Crysdot
  • 1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride 95+%
  • 1g
  • $ 431.00
  • Chemenu
  • 1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride 95%
  • 1g
  • $ 407.00
  • A1 Biochem Labs
  • 1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride 95%
  • 1 g
  • $ 500.00
Total 3 raw suppliers
Chemical Property of 1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride Edit
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride

There total 3 articles about 1-(4-Bromophenyl)-3-(piperidin-4-yl)ureahydrochloride 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 hydrogenchloride; In ethyl acetate; at 20 ℃;
DOI:10.1021/acs.jmedchem.7b01051
Guidance literature:
Multi-step reaction with 2 steps
1.1: N-ethyl-N,N-diisopropylamine / toluene / 0.67 h / 0 - 20 °C
1.2: 20 °C
2.1: hydrogenchloride / ethyl acetate / 20 °C
With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In ethyl acetate; toluene;
DOI:10.1021/acs.jmedchem.7b01051
Guidance literature:
Multi-step reaction with 2 steps
1.1: N-ethyl-N,N-diisopropylamine / toluene / 0.67 h / 0 - 20 °C
1.2: 20 °C
2.1: hydrogenchloride / ethyl acetate / 20 °C
With hydrogenchloride; N-ethyl-N,N-diisopropylamine; In ethyl acetate; toluene;
DOI:10.1021/acs.jmedchem.7b01051
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