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4-Nitrobenzyl carbanilate

Base Information
  • Chemical Name:4-Nitrobenzyl carbanilate
  • CAS No.:74109-32-3
  • Molecular Formula:C14H12 N2 O4
  • Molecular Weight:272.25608
  • Hs Code.:
  • European Community (EC) Number:667-587-9
  • ChEMBL ID:CHEMBL174673
  • Nikkaji Number:J3.600.593I
  • Mol file:74109-32-3.mol
4-Nitrobenzyl carbanilate

Synonyms:CHEMBL174673;SCHEMBL10490780;4-NITROBENZYL CARBANILATE;AKOS024334287

Suppliers and Price of 4-Nitrobenzyl carbanilate
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 3 raw suppliers
Chemical Property of 4-Nitrobenzyl carbanilate
Chemical Property:
  • Melting Point:121 - 123 °C 
  • PSA:84.15000 
  • LogP:3.93970 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:272.07970687
  • Heavy Atom Count:20
  • Complexity:329
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)NC(=O)OCC2=CC=C(C=C2)[N+](=O)[O-]
Technology Process of 4-Nitrobenzyl carbanilate

There total 3 articles about 4-Nitrobenzyl carbanilate 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 hydrogencarbonate; In ethyl acetate; at 0 ℃; for 0.25h;
Guidance literature:
With cobalt(II) iodide; zinc; tris(p-dimethylaminophenyl)phosphine; In toluene; at 120 ℃; for 40h; Schlenk technique; Inert atmosphere; Glovebox;
DOI:10.1039/c9ob00924h
Guidance literature:
Benzohydroxamic acid; With dmap; ethyl 2-(tert-butoxycarbonyloxyimino)-2-cyanoacetate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 0.25h; Green chemistry;
4-nitrobenzyl chloride; In dichloromethane; at 60 ℃; for 6h; chemoselective reaction; Green chemistry;
DOI:10.1002/adsc.201600661
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