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N-Methyl-4-tert-butylbenzylaMine Hydrochloride

Base Information Edit
  • Chemical Name:N-Methyl-4-tert-butylbenzylaMine Hydrochloride
  • CAS No.:101846-35-9
  • Molecular Formula:C12H19N*ClH
  • Molecular Weight:213.75
  • Hs Code.:
  • Mol file:101846-35-9.mol
N-Methyl-4-tert-butylbenzylaMine Hydrochloride

Synonyms:N-4-(1,1-Dimethylethyl)-N-methyl-benzolmethanamin hydrochlorid

Suppliers and Price of N-Methyl-4-tert-butylbenzylaMine Hydrochloride
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
  • Usbiological
  • N-Methyl-4-tert-butylbenzylamine Hydrochloride
  • 100mg
  • $ 460.00
  • TRC
  • N-Methyl-4-tert-butylbenzylamineHydrochloride
  • 1g
  • $ 1260.00
  • Medical Isotopes, Inc.
  • N-Methyl-4-tert-butylbenzylamineHCl
  • 100 mg
  • $ 650.00
Total 2 raw suppliers
Chemical Property of N-Methyl-4-tert-butylbenzylaMine Hydrochloride Edit
Chemical Property:
Purity/Quality:

98% *data from raw suppliers

N-Methyl-4-tert-butylbenzylamine Hydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses N-Methyl-4-tert-butylbenzylamine Hydrochloride, can be used as an intermediate for the synthesis of Butenafine and it’s derivatives, acting as an antifungal.
Technology Process of N-Methyl-4-tert-butylbenzylaMine Hydrochloride

There total 1 articles about N-Methyl-4-tert-butylbenzylaMine Hydrochloride 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 sodium bis(2-methoxyethoxy)aluminium dihydride; In toluene; for 1h; Ambient temperature;
DOI:10.1002/ardp.19933260607
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine / toluene / 1 h / Ambient temperature
2: 72 percent / Red-AlR / toluene / 1 h / Ambient temperature
With triethylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; In toluene;
DOI:10.1002/ardp.19933260608
Refernces Edit
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