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1-(Propyltriethoxyl)-3-methylimidazolium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

338741-79-0

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338741-79-0 Usage

Chemical family

Imidazolium salts

Physical state

Hygroscopic, colorless liquid

Odor

Strong

Solubility

Highly soluble in water

Common use

Ionic liquid in industrial processes

Application areas

Catalysis, electrochemistry, and organic synthesis

Performance enhancement

Stabilizes and enhances the performance of different reactions

Additive value

Valuable additive in various chemical processes

Environmental potential

Potential application in environmental remediation

Green solvent

Low volatility and low toxicity
These properties make 1-(Propyltriethoxyl)-3-methylimidazolium chloride a versatile and valuable compound in the field of chemistry and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 338741-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,7,4 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 338741-79:
(8*3)+(7*3)+(6*8)+(5*7)+(4*4)+(3*1)+(2*7)+(1*9)=170
170 % 10 = 0
So 338741-79-0 is a valid CAS Registry Number.

338741-79-0Downstream Products

338741-79-0Relevant academic research and scientific papers

Magnetic nanoparticles supported N-heterocyclic palladium complex: Synthesis and catalytic evaluations in Suzuki cross-coupling reaction

Dong, Yahao,Xue, Fengjun,Wei, Yuping

, (2021/03/04)

Because of the robustness and magnetic properties, the magnetic materials are promising and alternative candidate for the fabrication of noble metal in chemical catalysis from the viewpoint of green chemistry. Accordingly, an eco-friendly magnetic palladium catalyst loaded on N-Methylimidazole functionalized Fe3O4@SiO2 nanoparticles (Fe3O4@SiO2-NMIM-Pd) has been designed and prepared in the present work. The resultant composite exhibited excellent catalytic activity towards the Suzuki cross-coupling reaction for the synthesis of the corresponding biaryls in good to excellent yields (up to 96%) under aerobic conditions. In particular, this catalyst could be easily recovered through magnetic separation in a few cycles. The as-prepared palladium complex showed advantages including high thermal stability, low toxicity, moisture and oxygen insensitivities in Suzuki reactions. More importantly, this study presents a catalysis system, which will provide the magnetic materials access to the potential applications in a wide range of green organic catalysis.

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