40908-37-0 Usage
Description
4-Acetamido-2,2,6,6-tetramethylpiperidine is an organic compound with a unique structure that features a piperidine ring with four methyl groups and an acetamido group at the 4-position. 4-ACETAMIDO-2,2,6,6-TETRAMETHYLPIPERIDINE has versatile chemical properties and can be utilized in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
4-Acetamido-2,2,6,6-tetramethylpiperidine is used as a reactant for the synthesis of selenium and sulfur derivatives with antifungal activity. These derivatives can be employed in the development of antifungal medications, targeting a wide range of fungal infections and contributing to improved treatment options for patients.
Used in Chemical Industry:
In the chemical industry, 4-Acetamido-2,2,6,6-tetramethylpiperidine serves as a reactant for the synthesis of oxidants, which are essential in various chemical reactions and processes. Its ability to participate in these reactions makes it a valuable component in the production of various chemical products.
Used in Cosmetic Industry:
4-Acetamido-2,2,6,6-tetramethylpiperidine is used as an antioxidant in the oxoammonium-salt form. Its antioxidant properties make it suitable for use in cosmetic products, where it can help protect against oxidative stress and maintain the stability and efficacy of the formulations.
Used in Synthesis of Bioactive Compounds:
4-Acetamido-2,2,6,6-tetramethylpiperidine is used as a reactant for the synthesis of alpha and beta-glycosides, which are important bioactive compounds with potential applications in pharmaceutical and biological research.
Used in Material Science:
In material science, 4-Acetamido-2,2,6,6-tetramethylpiperidine is used as a reactant for the reaction of nitroxyl radicals with metal carbonyls. This reaction can lead to the formation of new materials with unique properties, contributing to the advancement of material science and the development of innovative applications.
Check Digit Verification of cas no
The CAS Registry Mumber 40908-37-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,0 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40908-37:
(7*4)+(6*0)+(5*9)+(4*0)+(3*8)+(2*3)+(1*7)=110
110 % 10 = 0
So 40908-37-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H22N2O/c1-8(14)12-9-6-10(2,3)13-11(4,5)7-9/h9,13H,6-7H2,1-5H3,(H,12,14)
40908-37-0Relevant articles and documents
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Alper
, p. 1417 (1973)
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A revised preparation of (4-Acetamido-2,2,6,6-tetramethylpiperidin-1-yl) oxyl and 4-acetamido-2,2,6,6-tetramethyl-1-oxopiperidinium tetrafluoroborate: Reagents for stoichiometric oxidations of alcohols
Tilley, Leon J.,Bobbitt, James M.,Murray, Stephanie A.,Camire, Casey E.,Eddy, Nicholas A.
, p. 326 - 329 (2013/03/14)
Revised preparations of (4-acetamido-2,2,6,6-tetramethylpiperidin-1-yl)oxyl and the corresponding oxoammonium salt, 4-acetamido-2,2,6,6-tetramethyl-1- oxoammonium tetrafluoroborate are presented together with some of the important properties of these two oxidizing reagents. Georg Thieme Verlag Stuttgart New York.
Synthesis of 2,2,6,6-tetramethylpiperidine derivatives
Kashparova,Kagan,Kashparov,Zhukova
, p. 667 - 668 (2007/10/03)
Diazotization of 4-amino-2,2,6,6-tetramethylpiperidine in acetic or sulfuric acid affords 2,2,6,6-tetramethyl-1,2,3,6-tetrahydropyridine in high yield. Under the same conditions, the corresponding nitroxyl radical transforms into 4-hydroxy-2,2,6,6-tetrame
