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4,5,6,7-Tetrachloro-2-hydroxy-isoindole-1,3-dione

Names

[ CAS No. ]:
85342-65-0

[ Name ]:
4,5,6,7-Tetrachloro-2-hydroxy-isoindole-1,3-dione

[Synonym ]:
N-hydroxy-3,4,5,6-tetrachlorophthalimide
4,5,6,7-Tetrachlor-2-hydroxy-isoindolin-1,3-dion
N-hydroxytetrachlorophtalimide
3,4,5,6-tetrachloro-N-hydroxyphthalimide
4,5,6,7-tetrachloro-2-hydroxy-isoindole-1,3-dione
4,5,6,7-tetrachloro-2-hydroxy-isoindoline-1,3-dione
N-hydroxytetrachlorophthalimide
tetrachloro-N-hydroxyphthalimide

Chemical & Physical Properties

[ Density]:
2.041g/cm3

[ Boiling Point ]:
532.1ºC at 760mmHg

[ Molecular Formula ]:
C8HCl4NO3

[ Molecular Weight ]:
300.91000

[ Flash Point ]:
275.6ºC

[ Exact Mass ]:
298.87100

[ PSA ]:
57.61000

[ LogP ]:
3.22330

[ Index of Refraction ]:
1.729

Safety Information

[ Symbol ]:

GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301

[ Precautionary Statements ]:
Missing Phrase - N15.00950417

[ RIDADR ]:
UN 2811 6.1 / PGIII

Synthetic Route

Precursor & DownStream

Articles

Efficient metal-free aerobic oxidation of aromatic hydrocarbons utilizing aryl-tetrahalogenated N-hydroxyphthalimides and 1,4-diamino-2,3-dichloroanthraquinone. Zhang Q, et al.

J. Chem. Technol. Biotechnol. 83(10) , 1364-1369, (2008)

Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.

Angew. Chem. Int. Ed. Engl. 55(33) , 9676-9, (2016)

A transformation analogous in simplicity and functional group tolerance to the venerable Suzuki cross-coupling between alkyl-carboxylic acids and boronic acids is described. This Ni-catalyzed reaction...

A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents.

Science 352(6287) , 801-5, (2016)

Alkyl carboxylic acids are ubiquitous in all facets of chemical science, from natural products to polymers, and represent an ideal starting material with which to forge new connections. This study dem...


More Articles


Related Compounds

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