Determine the necessary mass, volume, or concentration for preparing a solution.
purum p.a., ≥98%(T) purum p.a. for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged 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 783 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application
Catalyst for: aerobic oxidation of primary alcohols 1,4-addition reactions Reagent for: Synthesis of phosphazene derivatives Constrictive binding interactions Intramolecular C-N cross coupling reactions Dehydrohalogenative polycondensation Promotes the efficient O -alkylation of alcohols to form mixed alkyl carbonates.
Other Notes
Used for preparing cesium carboxylates which react with halogenides to give esters and lactones ; Used for an analogous preparation of thio ethers
| Pubchem Sid | 528774281 |
|---|---|
| Sorrisos canónicos | C(=O)([O-])[O-].[Cs+].[Cs+] |
| IUPAC Name | dicesium;carbonate |
| InChIKey | FJDQFPXHSGXQBY-UHFFFAOYSA-L |
| INCHI | 1S/CH2O3.2Cs/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2 |
| SMILES isoméricas | C(=O)([O-])[O-].[Cs+].[Cs+] |
| WGK Alemanha | 2 |
| RTECS | FK9400000 |
| Peso molecular | 325.82 |
| Beilstein | 4546405 |
| Reaxy-Rn | 4546405 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4546405&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 | Organic acids and derivatives |
| Classe | Organic carbonic acids and derivatives |
| Subclass | Organic carbonic acids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organic carbonic acids |
| Alternative Parents | Carbonate salts Organic alkali metal salts Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carbonate salt - Carbonic acid - Organic alkali metal salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Descrição | This compound belongs to the class of organic compounds known as organic carbonic acids. These are compounds comprising the carbonic acid functional group. |
| External Descriptors | Not available |
| Ponto de fusão (°C) | 610°C |
|---|---|
| Peso molecular | 325.820 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 325.796 Da |
| Monoisotopic Mass | 325.796 Da |
| Topological Polar Surface Area | 63.200 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 18.800 |
| 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 | 3 |
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