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2,2,4,5,5-Pentamethyl-2,5-dihydro-1H-imidazole is an organic compound with the chemical formula C7H13N2. It is a colorless liquid with a molecular weight of 125.19 g/mol. 2,2,4,5,5-Pentamethyl-2,5-dihydro-1H-imidazole is a derivative of imidazole, a heterocyclic aromatic organic compound containing a diazole ring. The structure of 2,2,4,5,5-Pentamethyl-2,5-dihydro-1H-imidazole features two methyl groups at the 2-position, one methyl group at the 4-position, and two methyl groups at the 5-position, with the imidazole ring being partially saturated. It is commonly used as a corrosion inhibitor, particularly in the oil and gas industry, due to its ability to form stable complexes with metal ions and protect metal surfaces from corrosion. Additionally, it has applications in various chemical processes and as a reagent in organic synthesis.

60829-51-8

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60829-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60829-51-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,2 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60829-51:
(7*6)+(6*0)+(5*8)+(4*2)+(3*9)+(2*5)+(1*1)=128
128 % 10 = 8
So 60829-51-8 is a valid CAS Registry Number.

60829-51-8Upstream product

60829-51-8Relevant academic research and scientific papers

Electrolytic Oxidation of Ketones in Ammoniacal Methanol in the Presence of Catalytic Amounts of KI

Chiba, Toshiro,Sakagami, Hirotoshi,Murata, Miki,Okimoto, Mitsuhiro

, p. 6764 - 6770 (1995)

The indirect electrooxidation of ketones in ammoniacal methanol using iodide ion as a mediator afforded 2,2-dialkyl-2,5-dihydro-1H-imidazoles 3 via an oxidative cyclocoupling of ketimine intermediates formed from ketones and ammonia.The treatment of 3 with dilute HCl gave α-amino ketone hydrochlorides 4 and the parent ketones in good yields.A similar electrooxidation of 3 resulted in the formation of the corresponding 2H-imidazoles 6, which were hydrolyzed to α-diketones and the parent ketones.The same products 6 could also conveniently be obtained by chemical oxidation of 3 with aqueous NaOCl.

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