phenyl N-(3-nitrophenyl)carbamate

Base Information

Chemical Name:phenyl N-(3-nitrophenyl)carbamate
CAS No.:50699-52-0
Molecular Formula:C13H10N2O4
Molecular Weight:258.233
Hs Code.:
European Community (EC) Number:666-984-4
DSSTox Substance ID:DTXSID60188777
Nikkaji Number:J2.108.180I
Wikidata:Q83060622
Mol file:50699-52-0.mol

Synonyms:phenyl N-(3-nitrophenyl)carbamate;50699-52-0;phenyl (3-nitrophenyl)carbamate;3-NITROPHENYL PHENYLCARBAMATE;35289-89-5;phenyl 3-nitrophenylcarbamate;phenyl(3-nitrophenyl)carbamate;SCHEMBL16672104;DTXSID60188777;AKOS001377991;UPCMLD0ENAT5817534:001;CS-0244087;N-(3-Nitrophenyl)carbamic acid phenyl ester;EN300-27176;Z31681648

Suppliers and Price of phenyl N-(3-nitrophenyl)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
PHENYL 3-NITROPHENYLCARBAMATE 95.00%
1G
$ 677.91

Total 2 raw suppliers

Chemical Property of phenyl N-(3-nitrophenyl)carbamate

Chemical Property:

PSA：84.15000
LogP:3.80190
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:258.06405680
Heavy Atom Count:19
Complexity:323

Purity/Quality:

99% ^*data from raw suppliers

PHENYL 3-NITROPHENYLCARBAMATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC(=O)NC2=CC(=CC=C2)[N+](=O)[O-]

Technology Process of phenyl N-(3-nitrophenyl)carbamate

There total 5 articles about phenyl N-(3-nitrophenyl)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:

: 1885-14-9
phenyl chloroformate

: 99-09-2
3-nitro-aniline

: 50699-52-0
(3-nitro-phenyl)-carbamic acid phenyl ester

Guidance literature:: In acetonitrile; at 25 ℃; Rate constant; Kinetics; Thermodynamic data; ΔH(excit.), ΔS(excit.); var. temp.;

Reference yield:

: 618-94-0
3-nitrobenzoic acid hydrazide

: 50699-52-0
(3-nitro-phenyl)-carbamic acid phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous sodium nitrite solution; acetic acid

2: petroleum ether

With acetic acid; Petroleum ether; sodium nitrite;