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2-Aminophenyl diethylcarbamate

Base Information
  • Chemical Name:2-Aminophenyl diethylcarbamate
  • CAS No.:88733-57-7
  • Molecular Formula:C11H16N2O2
  • Molecular Weight:208.26
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10521135
  • Wikidata:Q82385443
2-Aminophenyl diethylcarbamate

Synonyms:2-Aminophenyl diethylcarbamate;88733-57-7;DTXSID10521135

Suppliers and Price of 2-Aminophenyl diethylcarbamate
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
Total 1 raw suppliers
Chemical Property of 2-Aminophenyl diethylcarbamate
Chemical Property:
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:208.121177757
  • Heavy Atom Count:15
  • Complexity:205
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCN(CC)C(=O)OC1=CC=CC=C1N
Technology Process of 2-Aminophenyl diethylcarbamate

There total 3 articles about 2-Aminophenyl diethylcarbamate 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 tetrahydroborate; copper(l) chloride; In methanol; at 20 ℃; for 0.5h;
DOI:10.1021/ol0506563
Guidance literature:
O-phenyl N,N-diethylcarbamate; With tert.-butyl lithium; In tetrahydrofuran; pentane; at -78 ℃; for 1h; Inert atmosphere;
With Triisopropyl borate; In tetrahydrofuran; pentane; at -78 - 20 ℃; Inert atmosphere;
With water; sodium hydroxide; hydroxylamine-O-sulfonic acid; In tetrahydrofuran; pentane; at 20 ℃; for 16h; regioselective reaction; Inert atmosphere;
DOI:10.1021/jo5025078
Guidance literature:
Multi-step reaction with 2 steps
1: 50 percent / NaNO2; (CF3CO)2O / acetonitrile / 10 h / -35 - 20 °C
2: 84 percent / CuCl; NaBH4 / methanol / 0.5 h / 20 °C
With sodium tetrahydroborate; trifluoroacetic anhydride; copper(l) chloride; sodium nitrite; In methanol; acetonitrile;
DOI:10.1021/ol0506563
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