dichloronickel,1,2-dimethoxyethane - ≥98% , CAS No.29046-78-4

CAS: 29046-78-4 Cat. No.: D299631 Summenformel: NiCl2:CH3OCH2CH2OCH3 Molekulargewicht: 219.72 EG-Nummer: 627-461-6 PubChem CID: 15773433
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GRADE & PURITY ≥98%
Synonyms
FT-0638826 | MFCD00013481 | A903139 | Dichloro(dimethoxyethane)nickel | dichloronickel,1,2-dimethoxyethane | dichloronickel;1,2-dimethoxyethane | OCMNCWNTDDVHFK-UHFFFAOYSA-L | nickel(II) chloride dimethoxyethane | SCHEMBL1486833 | nicl2(dme) | NICKEL(II)
Storage
Store at 2-8°C,Protected from light,Argon charged
Shipped In
Wet ice
★
Size
Deutschland (EU)
USA*
Price
Qty
1g
D299631-1g
—
1 Auf Lager
25,95€
5g
D299631-5g
Auf Bestellung · 8–12 Wochen

62,39€

86,69€
Speichern 24,30 € (28.03%)
10g
D299631-10g
—
1 Auf Lager

82,35€

138,75€
Speichern 56,40 € (40.65%)
25g
D299631-25g
—
1 Auf Lager

169,12€

277,59€
Speichern 108,47 € (39.07%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

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.

Specifications

Synonyme
FT-0638826 | MFCD00013481 | A903139 | Dichloro(dimethoxyethane)nickel | dichloronickel,1,2-dimethoxyethane | dichloronickel;1,2-dimethoxyethane | OCMNCWNTDDVHFK-UHFFFAOYSA-L | nickel(II) chloride dimethoxyethane | SCHEMBL1486833 | nicl2(dme) | NICKEL(II)
Spezifikationen & Reinheit
≥98%
Storage
Store at 2-8°C,Protected from light,Argon charged
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥98%
Product Line
D299631-1g
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508814385
Kanonisches Lächeln
COCCOC.Cl[Ni]Cl
IUPAC Name
dichloronickel;1,2-dimethoxyethane
InChIKey
OCMNCWNTDDVHFK-UHFFFAOYSA-L
INCHI
1S/C4H10O2.2ClH.Ni/c1-5-3-4-6-2;;;/h3-4H2,1-2H3;2*1H;/q;;;+2/p-2
Isomere SMILES
COCCOC.Cl[Ni]Cl
WGK Deutschland
3
PubChem CID
15773433
Molekulargewicht
219.72

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
KlasseOrganooxygen compounds
SubclassEthers
Intermediate Tree Nodes Not available
Direct ParentDialkyl ethers
Alternative Parents Organic transition metal salts  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Organic metal salt - Organic transition metal salt - Dialkyl ether - Hydrocarbon derivative - Aliphatic acyclic compound
BeschreibungThis 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
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot NumberCertificate TypeDatumArtikel
A2517345Certificate of AnalysisDec 28, 2024 D299631
A2517346Certificate of AnalysisDec 28, 2024 D299631
B2506795Certificate of AnalysisDec 28, 2024 D299631
B2506796Certificate of AnalysisDec 28, 2024 D299631
B2626151Certificate of AnalysisDec 28, 2024 D299631
F2415301Certificate of AnalysisMar 30, 2024 D299631
F2415303Certificate of AnalysisMar 30, 2024 D299631
C2412031Certificate of AnalysisJul 07, 2022 D299631
H2217285Certificate of AnalysisJul 07, 2022 D299631
H2217801Certificate of AnalysisJul 07, 2022 D299631
H2217804Certificate of AnalysisJul 07, 2022 D299631
Chemische und physikalische Eigenschaften
EmpfindlichkeitHygroscopic;light and moisture and heat sensitive
Schmelzpunkt (°C)>300 °C
Molekulargewicht219.720 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count3
Exact Mass217.941 Da
Monoisotopic Mass217.941 Da
Topological Polar Surface Area18.500 Ų
Heavy Atom Count9
Formal Charge0
Complexity20.300
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
FAQs und Artikel
Organic Photoredox Catalysts for Visible Light-Driven Polymer and Small Molecule Synthesis
Photoredox Iridium Catalyst for Single Electron Transfer (SET) Cross-Coupling
Experimental Judgment and Condition Selection for Visible-Light Catalysis in Organic Synthesis
Experimental Judgment and Condition Selection for Visible-Light Catalysis in Organic Synthesis
Sulfonyl Hydrazide-Mediated Introduction of Small C(sp³) Fragments: Nickel-Catalyzed Cross-Coupling, Medicinal Chemistry Applications, and Reagent Selection
Construction and Transformation of Aziridines in Drug Synthesis: Ring Strain, N-Substituent Control, Selective Ring Opening, and Scaffold Expansion
Bond-Forming Reactions of N-Sulfinylamine and the Synthesis of S(VI) Functional Groups: Two-Electron Addition, Radical Addition, and Formal Cycloaddition
Kinetic Matching in Photoredox/Nickel C(sp²)–C(sp³) Coupling: Radical Generation, Nickel-Species Stability, and Photon Flux
Screening and Replacement of Green Solvents in Metallaphotoredox Catalysis: Reaction Compatibility and Process Feasibility
Citations of This Product
Lösungsrechner
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