≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
N-Hydroxytetrachlorophthalimide is used in the photoinduced decarboxylative borylation of redox-activated aryl N-hydroxyphthalimide esters to give aryl boronic esters.
| Pubchem Sid | 488189285 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488189285 |
| Sonrisas canónicas | C12=C(C(=C(C(=C1Cl)Cl)Cl)Cl)C(=O)N(C2=O)O |
| IUPAC Name | 4,5,6,7-tetrachloro-2-hydroxyisoindole-1,3-dione |
| InChIKey | UTRBHXSKVVPTLY-UHFFFAOYSA-N |
| INCHI | 1S/C8HCl4NO3/c9-3-1-2(4(10)6(12)5(3)11)8(15)13(16)7(1)14/h16H |
| Isómeros SMILES | C12=C(C(=C(C(=C1Cl)Cl)Cl)Cl)C(=O)N(C2=O)O |
| Peso molecular | 300.9 |
| Reaxy-Rn | 236019 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=236019&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Clase | Isoindoles and derivatives |
| Subclass | Isoindolines |
| Intermediate Tree Nodes | Isoindolones |
| Direct Parent | Phthalimides |
| Alternative Parents | Isoindoles Benzenoids Aryl chlorides Vinylogous halides Hydroxamic acids Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Phthalimide - Isoindole - Aryl chloride - Aryl halide - Benzenoid - Vinylogous halide - Hydroxamic acid - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 C2314678 | Certificate of Analysis | Feb 07, 2023 | H401609 |
| C2314680 | Certificate of Analysis | Feb 07, 2023 | H401609 |
| C2314684 | Certificate of Analysis | Feb 07, 2023 | H401609 |
| C2314725 | Certificate of Analysis | Feb 07, 2023 | H401609 |
| C2315151 | Certificate of Analysis | Feb 07, 2023 | H401609 |
| C2506073 | Certificate of Analysis | Feb 07, 2023 | H401609 |
| Solubilidad | DMSO (Slightly), Methanol (Slightly) |
|---|---|
| Sensibilidad | Moisture&Heat sensitive |
| Punto de fusión (°C) | 254 °C |
| Peso molecular | 300.900 g/mol |
| XLogP3 | 2.900 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 300.868 Da |
| Monoisotopic Mass | 298.871 Da |
| Topological Polar Surface Area | 57.600 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 320.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
