Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light,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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application:
Nickel(II) chloride ethylene glycol dimethyl ether complex can be used:
As a catalyst for the borylation of racemic benzylic chloride to synthesize enantioenriched benzylic boronic esters.
As a promoter for the trifluoromethylation of alkyl iodides to synthesize broad range of alkyl-CF3 compounds.
For the synthesis of nickel bis(benzimidazol-2-ylidene) pincer complexes which can be used for electrocatalytic reduction of CO2 to CO.
As a Lewis acid catalyst for C-acylation β-ketoesters through photoactivation by visible light.
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 oxygen compounds |
| Classe | Organooxygen compounds |
| Subclass | Ethers |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkyl ethers |
| Alternative Parents | Organic transition metal salts Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Organic metal salt - Organic transition metal salt - Dialkyl ether - Hydrocarbon derivative - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Dec 28, 2024 | D299631 | |
| Certificate of Analysis | Dec 28, 2024 | D299631 | |
| Certificate of Analysis | Dec 28, 2024 | D299631 | |
| Certificate of Analysis | Dec 28, 2024 | D299631 | |
| Certificate of Analysis | Dec 28, 2024 | D299631 | |
| Certificate of Analysis | Mar 30, 2024 | D299631 | |
| Certificate of Analysis | Mar 30, 2024 | D299631 | |
| Certificate of Analysis | Jul 07, 2022 | D299631 | |
| Certificate of Analysis | Jul 07, 2022 | D299631 | |
| Certificate of Analysis | Jul 07, 2022 | D299631 | |
| Certificate of Analysis | Jul 07, 2022 | D299631 |
| Sensibilità | Hygroscopic;light and moisture and heat sensitive |
|---|---|
| Punto di fusione (°C) | >300 °C |
| Peso molecolare | 219.720 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 217.941 Da |
| Monoisotopic Mass | 217.941 Da |
| Topological Polar Surface Area | 18.500 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 20.300 |
| 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 | 2 |