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N-(1-(naphthalen-1-yl)ethyl)forMaMide

Base Information Edit
  • Chemical Name:N-(1-(naphthalen-1-yl)ethyl)forMaMide
  • CAS No.:49681-33-6
  • Molecular Formula:C13H13NO
  • Molecular Weight:199.252
  • Hs Code.:
  • Mol file:49681-33-6.mol
N-(1-(naphthalen-1-yl)ethyl)forMaMide

Synonyms:Formamide, N-[1-(1-naphthalenyl)ethyl]-, (±)-;Formamide, N-[1-(1-naphthalenyl)ethyl]-;

Suppliers and Price of N-(1-(naphthalen-1-yl)ethyl)forMaMide
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
  • TRC
  • N-[1-(1-Naphthalenyl)ethyl]formamide
  • 1g
  • $ 230.00
  • TRC
  • N-[1-(1-Naphthalenyl)ethyl]formamide
  • 500mg
  • $ 120.00
Total 7 raw suppliers
Chemical Property of N-(1-(naphthalen-1-yl)ethyl)forMaMide Edit
Chemical Property:
  • Boiling Point:420.7±24.0 °C(Predicted) 
  • PKA:15.43±0.23(Predicted) 
  • PSA:29.10000 
  • Density:1.108±0.06 g/cm3(Predicted) 
  • LogP:3.67360 
Purity/Quality:

≥95% *data from raw suppliers

N-[1-(1-Naphthalenyl)ethyl]formamide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses N-[1-(1-Naphthalenyl)ethyl]formamide is derived from 1-Acetylnaphthalene (A186940), which is used in the preparation of S(-)-1-(1''-naphthyl) ethanol, an important synthetic intermediate of mevinic acid analog;Also, it is used in the preparation of (R)-(+)-1-(1-naphthyl)ethylamine as an intermediate of cinacalcet.
Technology Process of N-(1-(naphthalen-1-yl)ethyl)forMaMide

There total 5 articles about N-(1-(naphthalen-1-yl)ethyl)forMaMide 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 1-methyl-1H-imidazole; [2,2]bipyridinyl; copper(l) iodide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen; In acetonitrile; at 60 ℃; for 20h; under 1125.11 Torr;
DOI:10.1002/cssc.201903266
Guidance literature:
With 1-methyl-1H-imidazole; [2,2]bipyridinyl; copper(l) iodide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen; In acetonitrile; at 60 ℃; for 20h; under 1125.11 Torr;
DOI:10.1002/cssc.201903266
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