Determine the necessary mass, volume, or concentration for preparing a solution.
2.0M in methylene chloride 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.
Description
Used in synthetic applications of carbon-substituted iminium saltsReactant for:Synthesis of mutasynthons added to cultures ofA. pretiosumfor mutasynthetic generation of ansamitocin derivativesOxalic acid formation from hydroxyl radical substitutionsCyclization to produce CRF1 receptor antagonistsPreparation, optical and electrochemical studies of thiophene end capped olig(2,3-alkylthieno[3,4-b]pyrazine)Asymmetrical synthesis of glycosyl chlorides and bromides
| Sonrisas canónicas | C(=O)(C(=O)Br)Br |
|---|---|
| IUPAC Name | oxalyl dibromide |
| InChIKey | JAZLVNXWYDFQFE-UHFFFAOYSA-N |
| INCHI | 1S/C2Br2O2/c3-1(5)2(4)6 |
| Isómeros SMILES | C(=O)(C(=O)Br)Br |
| WGK Alemania | 3 |
| Número ONU | 2922 |
| Grupo de embalaje | I |
| Peso molecular | 215.83 |
| Beilstein | 1744440 |
| Reaxy-Rn | 1744437 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1744437&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 | Organohalogen compounds |
| Clase | Acyl halides |
| Subclass | Acyl bromides |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acyl bromides |
| Alternative Parents | Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acyl bromide - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organobromide - Carbonyl group - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as acyl bromides. These are organic compounds containing the functional group -CO-Br. |
| External Descriptors | Not available |
| Punto de ebullición (°C) | 16-17°C/10mmHg |
|---|---|
| Punto de fusión (°C) | -19 °C |
| Peso molecular | 215.830 g/mol |
| XLogP3 | 1.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 215.824 Da |
| Monoisotopic Mass | 213.827 Da |
| Topological Polar Surface Area | 34.100 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 75.500 |
| 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 |