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338741-79-0

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338741-79-0 Usage

General Description

1-(Propyltriethoxyl)-3-methylimidazolium chloride is a type of organic compound that belongs to the family of imidazolium salts. It is a hygroscopic, colorless liquid with a strong odor and is highly soluble in water. This chemical is commonly used as an ionic liquid in various industrial processes, such as in catalysis, electrochemistry, and as a solvent for organic synthesis. It is known for its ability to stabilize and enhance the performance of different reactions due to its unique properties, making it a valuable additive in various chemical processes. Additionally, it has attracted attention for its potential application in environmental remediation and as a green solvent due to its low volatility and low toxicity.

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 articles and documents

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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