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5-Amino-2-chloro-4-fluorophenyl methyl carbonate

Base Information Edit
  • Chemical Name:5-Amino-2-chloro-4-fluorophenyl methyl carbonate
  • CAS No.:110957-08-9
  • Molecular Formula:C8H7ClFNO3
  • Molecular Weight:219.6
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30445061
  • Wikidata:Q82263390
  • Mol file:110957-08-9.mol
5-Amino-2-chloro-4-fluorophenyl methyl carbonate

Synonyms:110957-08-9;5-Amino-2-chloro-4-fluorophenyl methyl carbonate;SCHEMBL8084592;DTXSID30445061;RVNOLDUNQMDIBG-UHFFFAOYSA-N;MFCD24624124;2-fluoro-4-chloro-5-methoxycarbonyloxianiline;2-fluoro-4-chloro-5-methoxycarbonyloxyaniline

Suppliers and Price of 5-Amino-2-chloro-4-fluorophenyl methyl carbonate
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
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Total 0 raw suppliers
Chemical Property of 5-Amino-2-chloro-4-fluorophenyl methyl carbonate Edit
Chemical Property:
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:3
  • Exact Mass:219.0098489
  • Heavy Atom Count:14
  • Complexity:217
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC(=O)OC1=C(C=C(C(=C1)N)F)Cl
Technology Process of 5-Amino-2-chloro-4-fluorophenyl methyl carbonate

There total 3 articles about 5-Amino-2-chloro-4-fluorophenyl methyl carbonate 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 hydrogen; platinum(IV) oxide; In ethanol; ethyl acetate; for 2h;
DOI:10.1021/jm990345w
Guidance literature:
Multi-step reaction with 3 steps
1: 99 percent / aq. NaOH / 0.25 h / 5 - 10 °C
2: 82 percent / HNO3; H2SO4 / 0.5 h / 30 °C
3: 82 percent / H2 / PtO2 / ethanol; ethyl acetate / 2 h
With sodium hydroxide; sulfuric acid; hydrogen; nitric acid; platinum(IV) oxide; In ethanol; ethyl acetate; 1: Acylation / 2: Nitration / 3: Reduction;
DOI:10.1021/jm990345w
Guidance literature:
Multi-step reaction with 2 steps
1: 82 percent / HNO3; H2SO4 / 0.5 h / 30 °C
2: 82 percent / H2 / PtO2 / ethanol; ethyl acetate / 2 h
With sulfuric acid; hydrogen; nitric acid; platinum(IV) oxide; In ethanol; ethyl acetate; 1: Nitration / 2: Reduction;
DOI:10.1021/jm990345w
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