4-Nitrophenyl ethylcarbamate

Base Information

Chemical Name:4-Nitrophenyl ethylcarbamate
CAS No.:17576-41-9
Molecular Formula:C₉H₁₀N₂O₄
Molecular Weight:210.189
Hs Code.:2924299090
DSSTox Substance ID:DTXSID40170019
Nikkaji Number:J48.404K
Wikidata:Q83039864
ChEMBL ID:CHEMBL2288439
Mol file:17576-41-9.mol

Synonyms:4-Nitrophenyl ethylcarbamate;17576-41-9;(4-nitrophenyl) N-ethylcarbamate;Ethylcarbamic Acid 4-Nitrophenyl Ester;CARBAMIC ACID, ETHYL-, 4-NITROPHENYL ESTER;BRN 1975958;AI3-27285;4-NITROPHENYL N-ETHYLCARBAMATE;4-Nitrophenylethylcarbamate;SCHEMBL1695035;CHEMBL2288439;DTXSID40170019;MFCD01738228;N-Ethylcarbamic acid 4-nitrophenyl ester;LS-49758;Carbamic acid, ethyl-, p-nitrophenyl ester;CS-0094883;D75660;CARBAMIC ACID,ETHYL-,4-NITROPHENYL ESTER

Suppliers and Price of 4-Nitrophenyl ethylcarbamate

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

TRC
EthylcarbamicAcid4-NitrophenylEster
25g
$ 1320.00

American Custom Chemicals Corporation
CARBAMIC ACID,ETHYL-,4-NITROPHENYL ESTER 95.00%
5MG
$ 500.01

Total 6 raw suppliers

Chemical Property of 4-Nitrophenyl ethylcarbamate

Chemical Property:

Vapor Pressure:0.000181mmHg at 25°C
Boiling Point:329.1°Cat760mmHg
Flash Point:152.9°C
PSA：87.64000
Density:1.279g/cm³
LogP:2.43070
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:210.06405680
Heavy Atom Count:15
Complexity:231

Purity/Quality:

98%+ ^*data from raw suppliers

EthylcarbamicAcid4-NitrophenylEster ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCNC(=O)OC1=CC=C(C=C1)[N+](=O)[O-]
Uses Ethylcarbamic Acid 4-Nitrophenyl Ester is used in the synthesis of cholesterol esterase inhibitory agents.

Technology Process of 4-Nitrophenyl ethylcarbamate

There total 2 articles about 4-Nitrophenyl ethylcarbamate 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: