≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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.
Product Describtion:
1,4-Diacetoxy-2-bromobenzene can be prepared by reacting 1,4-benzoquinone with zinc bromide in the presence of acetic anhydride.1,4-Diacetoxy-2-bromobenzene may be used to synthesize bromohydroquinone and (Sp,S)-1-(2,5-diacetoxyphenyl)-2-(p-tolylsulfinyl)ferrocene.
Product Application:
1,4-Diacetoxy-2-bromobenzene may be used to synthesize bromohydroquinone and (Sp,S)-1-(2,5-diacetoxyphenyl)-2-(p-tolylsulfinyl)ferrocene.
| Pubchem Sid | 504762522 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504762522 |
| Canonical Smiles | CC(=O)OC1=CC(=C(C=C1)OC(=O)C)Br |
| IUPAC Name | (4-acetyloxy-3-bromophenyl) acetate |
| InChIKey | XRIFNWOHWJOCQG-UHFFFAOYSA-N |
| INCHI | 1S/C10H9BrO4/c1-6(12)14-8-3-4-10(9(11)5-8)15-7(2)13/h3-5H,1-2H3 |
| Isomeric SMILES | CC(=O)OC1=CC(=C(C=C1)OC(=O)C)Br |
| WGK Germany | 3 |
| Molecular Weight | 273.08 |
| Reaxy-Rn | 2053249 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2053249&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 | Benzenoids |
| Class | Phenol esters |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenol esters |
| Alternative Parents | Phenoxy compounds Bromobenzenes Dicarboxylic acids and derivatives Aryl bromides Carboxylic acid esters Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenol ester - Phenoxy compound - Bromobenzene - Halobenzene - Aryl bromide - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Aryl halide - Carboxylic acid ester - Carboxylic acid derivative - Organic oxygen compound - Organooxygen compound - Organobromide - Organohalogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group. |
| 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 |
|---|---|---|---|
 F23251131 | Certificate of Analysis | Apr 02, 2026 | D469310 |
| F23251139 | Certificate of Analysis | Apr 02, 2026 | D469310 |
| F23251142 | Certificate of Analysis | Apr 02, 2026 | D469310 |
| F23251147 | Certificate of Analysis | Apr 02, 2026 | D469310 |
| Melt Point(°C) | 70-75 °C (lit.) |
|---|---|
| Molecular Weight | 273.080 g/mol |
| XLogP3 | 2.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 4 |
| Exact Mass | 271.968 Da |
| Monoisotopic Mass | 271.968 Da |
| Topological Polar Surface Area | 52.600 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 254.000 |
| 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 |
