Ethyl 4-[[methyl(nitroso)carbamoyl]amino]benzoate

Base Information

Chemical Name:Ethyl 4-[[methyl(nitroso)carbamoyl]amino]benzoate
CAS No.:91332-70-6
Molecular Formula:C₁₁H₁₃N₃O₄
Molecular Weight:251.242
Hs Code.:
NSC Number:72719
DSSTox Substance ID:DTXSID50291042
Wikidata:Q82028872

Synonyms:91332-70-6;ethyl 4-[[methyl(nitroso)carbamoyl]amino]benzoate;NSC72719;DTXSID50291042;NSC-72719

Suppliers and Price of Ethyl 4-[[methyl(nitroso)carbamoyl]amino]benzoate

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 4 raw suppliers

Chemical Property of Ethyl 4-[[methyl(nitroso)carbamoyl]amino]benzoate

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.26g/cm³
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:251.09060590
Heavy Atom Count:18
Complexity:313

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=CC=C(C=C1)NC(=O)N(C)N=O

Technology Process of Ethyl 4-[[methyl(nitroso)carbamoyl]amino]benzoate

There total 2 articles about Ethyl 4-[[methyl(nitroso)carbamoyl]amino]benzoate 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:

Reference yield:

: 94-09-7
p-aminoethylbenzoate

: 91332-70-6
N-Nitroso-N-methyl-N'-(4-ethoxycarbonyl-phenyl)-harnstoff

Guidance literature:: Multi-step reaction with 2 steps

1: CHCl₃

2: aq. NaNO₂, HCO₂H

With formic acid; sodium nitrite; In chloroform;
DOI:10.1021/jm00342a010