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2,2,6,6-Tetramethyl-4-phenyliminopiperidine is a complex organic compound with the chemical formula C17H26N2. It is a derivative of piperidine, a heterocyclic amine, and features a phenyl group attached to the imine functionality. 2,2,6,6-tetramethyl-4-phenyliminopiperidine is characterized by its four methyl groups (CH3) at the 2, 2, 6, and 6 positions, which contribute to its steric hindrance and overall structure. It is often used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties and reactivity. The compound's structure and properties make it a valuable intermediate in the development of new drugs and other chemical products.

52098-47-2

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52098-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52098-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,9 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 52098-47:
(7*5)+(6*2)+(5*0)+(4*9)+(3*8)+(2*4)+(1*7)=122
122 % 10 = 2
So 52098-47-2 is a valid CAS Registry Number.

52098-47-2Relevant articles and documents

PREPARATION OF 2,2,6,6-TETRAMETHYL-4-AMINOPIPERIDINE AND ITS SUBSTITUTED COMPOUNDS BY ELECTROREDUCTION OF AZOMETHINES OF 2,2,6,6-TETRAMETHYL-4-OXOPIPERIDINE (TRIACETONAMINE)

Fioshin, M. Ya.,Avrutskaya, I. A.,Surov, I. I.,Novikov, V. T.

, p. 182 - 191 (2007/10/02)

Five methods have been developed for electrosynthesis of 2,2,6,6-tetramethyl-4-aminopiperidine in 95 - 98 percent yield via the lead-cathode reduction of 2,2,6,6-tetramethyl-4-oxiimino-piperidine, a mixture of triacetonamine with inorganic salts of hydroxylamine, and a mixture of triacetonamine with nitric acid in a solution of sulphuric acid, via the reduction of azine triacetonamine and of a mixture of triacetonamine with inorganic salts of hydrazine in a neutral solution.The corresponding saturated derivatives of 2,2,6,6-tetramethyl-4-aminopiperidine have been obtained in 60 - 80 percent yield by ele ctroreduction of phenylimine and ethylene diimine.

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