4-Nitrophenyl-N-(2-chloroethyl)carbamate

Base Information

Chemical Name:4-Nitrophenyl-N-(2-chloroethyl)carbamate
CAS No.:55661-43-3
Molecular Formula:C9H8 Cl N3 O5
Molecular Weight:273.633
Hs Code.:
DSSTox Substance ID:DTXSID10971015
Nikkaji Number:J67.551B
Wikidata:Q82954432
ChEMBL ID:CHEMBL50202
Mol file:55661-43-3.mol

Synonyms:4-nitrophenyl-N-(2-chloroethyl)carbamate;NPCEC

Suppliers and Price of 4-Nitrophenyl-N-(2-chloroethyl)carbamate

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

American Custom Chemicals Corporation
4-NITROPHENYL-N-(2-CHLOROETHYL)CARBAMATE 95.00%
5MG
$ 497.43

Total 4 raw suppliers

Chemical Property of 4-Nitrophenyl-N-(2-chloroethyl)carbamate

Chemical Property:

Vapor Pressure:1.82E-06mmHg at 25°C
Melting Point:114-116 °C(Solv: ethanol (64-17-5))
Boiling Point:395.6°Cat760mmHg
PKA:-3.53±0.70(Predicted)
Flash Point:193°C
PSA：104.79000
Density:1.51g/cm³
LogP:2.83900
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:273.0152481
Heavy Atom Count:18
Complexity:314

Purity/Quality:

99% ^*data from raw suppliers

4-NITROPHENYL-N-(2-CHLOROETHYL)CARBAMATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1[N+](=O)[O-])OC(=O)N(CCCl)N=O

Technology Process of 4-Nitrophenyl-N-(2-chloroethyl)carbamate

There total 3 articles about 4-Nitrophenyl-N-(2-chloroethyl)carbamate 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: 92.7%

: 55661-43-3
p-nitrophenyl N-(2-chloroethyl)-N-nitroso-carbamate

Guidance literature:

Reference yield: 90.0%

: 55661-42-2
N-(chloro-2 ethyl) carbamate de p. nitrophenyle

: 55661-43-3
p-nitrophenyl N-(2-chloroethyl)-N-nitroso-carbamate

Guidance literature:: With pyridine; nitrosylchloride;

Reference yield:

: 100-02-7,78813-13-5,89830-32-0
4-nitro-phenol

: 55661-43-3
p-nitrophenyl N-(2-chloroethyl)-N-nitroso-carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / pyridine / 3 h / Ambient temperature

2: 85 percent / NOCl, Et₃N / ethyl acetate / 2 h

With nitrosylchloride; triethylamine; In pyridine; ethyl acetate;
DOI:10.1002/jps.2600770218