Phthalimide, N-(m-nitrobenzyloxy)-

Base Information

Chemical Name:Phthalimide, N-(m-nitrobenzyloxy)-
CAS No.:30777-84-5
Molecular Formula:C15H10 N2 O5
Molecular Weight:298.255
Hs Code.:2925190090
NSC Number:130679
DSSTox Substance ID:DTXSID60184794
Nikkaji Number:J50.524B
Wikidata:Q83055736
Mol file:30777-84-5.mol

Synonyms:30777-84-5;Phthalimide, N-(m-nitrobenzyloxy)-;N-(m-Nitrobenzyloxy)phthalimide;2-[(3-nitrophenyl)methoxy]isoindole-1,3-dione;2-((3-nitrobenzyl)oxy)isoindoline-1,3-dione;N-[(3-Nitrophenyl)methoxy]phthalimide;NSC 130679;BRN 1494011;NSC130679;SCHEMBL5532596;N-(3-nitrobenzyloxy)phthalimide;DTXSID60184794;MXLWOFFKIKAHTG-UHFFFAOYSA-N;1H-Isoindole-1,3(2H)-dione, 2-((3-nitrophenyl)methoxy)-;NSC-130679;1H-Isoindole-1, 2-[(3-nitrophenyl)methoxy]-;2-[(3-nitrophenyl)methoxy]-2,3-dihydro-1H-isoindole-1,3-dione

Suppliers and Price of Phthalimide, N-(m-nitrobenzyloxy)-

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 Phthalimide, N-(m-nitrobenzyloxy)-

Chemical Property:

Vapor Pressure:3.93E-10mmHg at 25°C
Boiling Point:500.1°Cat760mmHg
Flash Point:256.2°C
PSA：92.43000
Density:1.5g/cm³
LogP:2.78370
XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:298.05897142
Heavy Atom Count:22
Complexity:451

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=O)N(C2=O)OCC3=CC(=CC=C3)[N+](=O)[O-]

Technology Process of Phthalimide, N-(m-nitrobenzyloxy)-

There total 4 articles about Phthalimide, N-(m-nitrobenzyloxy)- 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: 45.0%

: 524-38-9
N-hydroxyphthalimide

: 3958-57-4
1-bromomethyl-3-nitrobenzene

: 30777-84-5
N-(3-nitro-benzyloxy)-phthalimide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 19h;

Reference yield:

: 524-38-9
N-hydroxyphthalimide

: 619-25-0
3-Nitrobenzyl alcohol

: 30777-84-5
N-(3-nitro-benzyloxy)-phthalimide

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 - 50 ℃;
DOI:10.1016/S0960-894X(03)00713-3

Reference yield:

: 524-38-9
N-hydroxyphthalimide

: 619-23-8
3-Nitrobenzyl chloride

: 30777-84-5
N-(3-nitro-benzyloxy)-phthalimide

Guidance literature:: With tetra(n-butyl)ammonium hydrogensulfate; sodium hydrogencarbonate; In dichloromethane; water; at 40 ℃;
DOI:10.24820/ark.5550190.p010.472