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3-Nitrophenyl methylcarbamate

Base Information
  • Chemical Name:3-Nitrophenyl methylcarbamate
  • CAS No.:6132-21-4
  • Molecular Formula:C8H8N2O4
  • Molecular Weight:196.163
  • Hs Code.:
  • NSC Number:55614
  • DSSTox Substance ID:DTXSID60210224
  • Nikkaji Number:J747.752J
  • Wikidata:Q83084836
  • ChEMBL ID:CHEMBL3249292
3-Nitrophenyl methylcarbamate

Synonyms:3-Nitrophenyl methylcarbamate;6132-21-4;Carbamic acid, methyl-, 3-nitrophenyl ester;Phenol, 3-nitro-, methylcarbamate;NSC 55614;TL-948;SCHEMBL4260502;CHEMBL3249292;DTXSID60210224;NSC55614;NSC-55614;Methylcarbamic acid 3-nitrophenyl ester;LS-50280;Methyl-carbamic acid 3-nitro-phenyl ester

Suppliers and Price of 3-Nitrophenyl methylcarbamate
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 6 raw suppliers
Chemical Property of 3-Nitrophenyl methylcarbamate
Chemical Property:
  • Vapor Pressure:0.00132mmHg at 25°C 
  • Boiling Point:297.8°C at 760 mmHg 
  • Flash Point:133.9°C 
  • Density:1.327g/cm3 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:196.04840674
  • Heavy Atom Count:14
  • Complexity:226
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CNC(=O)OC1=CC=CC(=C1)[N+](=O)[O-]
Technology Process of 3-Nitrophenyl methylcarbamate

There total 2 articles about 3-Nitrophenyl methylcarbamate 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 triethylamine; In dichloromethane; at 20 ℃; for 4h;
Guidance literature:
m-Nitrophenol, Methylisocyanat;
Guidance literature:
With hydrogen; palladium 10% on activated carbon; In methanol; at 20 ℃;
upstream raw materials:

meta-nitrophenol

methyl isocyanate

Downstream raw materials:

N-methyl-3-aminophenylcarbamate

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