Determine the necessary mass, volume, or concentration for preparing a solution.
≥97%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged,Room temperature Ships Normal 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488183810 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183810 |
| Canonical Smiles | C1=CC2=C(C=C1Br)C(=O)OC2=O |
| IUPAC Name | 5-bromo-2-benzofuran-1,3-dione |
| InChIKey | BCKVHOUUJMYIAN-UHFFFAOYSA-N |
| INCHI | 1S/C8H3BrO3/c9-4-1-2-5-6(3-4)8(11)12-7(5)10/h1-3H |
| Isomeric SMILES | C1=CC2=C(C=C1Br)C(=O)OC2=O |
| Molecular Weight | 227.01 |
| Beilstein | 17485 |
| Reaxy-Rn | 131285 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=131285&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 |
| Class | Benzofurans |
| Subclass | Benzofuranones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phthalic anhydrides |
| Alternative Parents | Isobenzofuranones Dicarboxylic acids and derivatives Benzenoids Aryl bromides Carboxylic acid anhydrides Oxacyclic compounds Organooxygen compounds Organobromides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Phthalic anhydride - Phthalic_anhydride - Isobenzofuranone - Isocoumaran - Aryl bromide - Aryl halide - Dicarboxylic acid or derivatives - Benzenoid - Carboxylic acid anhydride - Carboxylic acid derivative - Oxacycle - Organohalogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organobromide - Organooxygen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as phthalic anhydrides. These are compounds containing a phthalic anhydride moiety (or a derivative thereof), which consists of a benzene fused to a furan-1,3-dione. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Apr 13, 2026 | B151972 | |
| Certificate of Analysis | Apr 13, 2026 | B151972 | |
| Certificate of Analysis | Apr 13, 2026 | B151972 | |
| Certificate of Analysis | Apr 13, 2026 | B151972 | |
| Certificate of Analysis | Apr 13, 2026 | B151972 | |
| Certificate of Analysis | Sep 08, 2025 | B151972 | |
| Certificate of Analysis | Sep 08, 2025 | B151972 | |
| Certificate of Analysis | Sep 11, 2023 | B151972 | |
| Certificate of Analysis | Jun 11, 2022 | B151972 | |
| Certificate of Analysis | Jun 11, 2022 | B151972 |
| Solubility | Very soluble in Benzene |
|---|---|
| Sensitivity | Moisture sensitive |
| Boil Point(°C) | 301°C |
| Melt Point(°C) | 106-110°C |
| Molecular Weight | 227.010 g/mol |
| XLogP3 | 2.000 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 225.927 Da |
| Monoisotopic Mass | 225.927 Da |
| Topological Polar Surface Area | 43.400 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 238.000 |
| 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 |
| 1. Chen Biao, Huang Wenhuan, Zhang Guoqing. (2023) Observation of Chiral-selective room-temperature phosphorescence enhancement via chirality-dependent energy transfer. Nature Communications, 14 (1): (1-8). [PMID:36934094] [10.1038/s41467-023-37157-w] |
| 2. Kaiyuan You, Hongyan Yao, Yunhe Zhang, Yu Liu, Shanyou Liu, Ying Song, Shaowei Guan. (2015) Phenylethynyl- and naphthylethynyl-terminated hyperbranched polyimides with low melt viscosity. HIGH PERFORMANCE POLYMERS, [PMID:] [10.1177/0954008315570398] |