1H-Isoindole-1,3(2H)-dione, 2-((6-iodo-4-oxo-4H-3,1-benzoxazin-2-yl)methyl)-

Base Information

Chemical Name:1H-Isoindole-1,3(2H)-dione, 2-((6-iodo-4-oxo-4H-3,1-benzoxazin-2-yl)methyl)-
CAS No.:134700-31-5
Molecular Formula:C17H9IN2O4
Molecular Weight:432.1688
Hs Code.:
DSSTox Substance ID:DTXSID80158871
Wikidata:Q83027157
Mol file:134700-31-5.mol

Synonyms:BRN 4762163;1H-Isoindole-1,3(2H)-dione, 2-((6-iodo-4-oxo-4H-3,1-benzoxazin-2-yl)methyl)-;134700-31-5;2-[(6-iodo-4-oxo-3,1-benzoxazin-2-yl)methyl]isoindole-1,3-dione;2-((6-Iodo-4-oxo-4H-3,1-benzoxazin-2-yl)methyl)-1H-isoindole-1,3(2H)-dione;CBMicro_029429;Oprea1_130584;DTXSID80158871;BIM-0029352.P001;SR-01000519398;SR-01000519398-1;5730-99-4

Suppliers and Price of 1H-Isoindole-1,3(2H)-dione, 2-((6-iodo-4-oxo-4H-3,1-benzoxazin-2-yl)methyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1H-Isoindole-1,3(2H)-dione, 2-((6-iodo-4-oxo-4H-3,1-benzoxazin-2-yl)methyl)-

Chemical Property:

Vapor Pressure:2.36E-13mmHg at 25°C
Boiling Point:577.9°C at 760 mmHg
Flash Point:303.3°C
Density:1.93g/cm³
XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:431.96070
Heavy Atom Count:24
Complexity:596

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=O)N(C2=O)CC3=NC4=C(C=C(C=C4)I)C(=O)O3

Technology Process of 1H-Isoindole-1,3(2H)-dione, 2-((6-iodo-4-oxo-4H-3,1-benzoxazin-2-yl)methyl)-

There total 1 articles about 1H-Isoindole-1,3(2H)-dione, 2-((6-iodo-4-oxo-4H-3,1-benzoxazin-2-yl)methyl)- 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:

: 6780-38-7
N-phthaloylglycine chloride

: 5326-47-6
2-amino-5-iodobenzoic acid

: 134700-31-5
2-(6-Iodo-4-oxo-4H-benzo[d][1,3]oxazin-2-ylmethyl)-isoindole-1,3-dione

Guidance literature:: With pyridine; 1) 0 to 5 deg C, 1h, 2) RT, overnight;

Reference yield: 75.0%

: 123-30-8
4-amino-phenol

: 134700-31-5
2-(6-Iodo-4-oxo-4H-benzo[d][1,3]oxazin-2-ylmethyl)-isoindole-1,3-dione

: 131357-87-4
2-[3-(4-Hydroxy-phenyl)-6-iodo-4-oxo-3,4-dihydro-quinazolin-2-ylmethyl]-isoindole-1,3-dione

Guidance literature:: With pyridine; Heating;

Reference yield:

: 134700-31-5
2-(6-Iodo-4-oxo-4H-benzo[d][1,3]oxazin-2-ylmethyl)-isoindole-1,3-dione

: 134700-43-9
2-[3-(3-Diethylaminomethyl-4-hydroxy-phenyl)-6-iodo-4-oxo-3,4-dihydro-quinazolin-2-ylmethyl]-isoindole-1,3-dione

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / pyridine / Heating

2: 1) EtOH, 1h, reflux, 2) 12h, reflux

With pyridine;