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2,2,5,5-tetramethyl-3-carbamido-1-hydroxypyrrolidine is a complex organic compound with the molecular formula C10H20N2O2. It is a derivative of pyrrolidine, a heterocyclic amine, and features four methyl groups (CH3) at the 2, 2, 5, and 5 positions, a carbamido group (CONH2) at the 3 position, and a hydroxyl group (OH) at the 1 position. 2,2,5,5-tetramethyl-3-carbamido-1-hydroxypyrrolidine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through multi-step organic reactions and is used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its solubility and stability, can be influenced by the presence of the functional groups and the overall molecular structure.

6916-96-7

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6916-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6916-96-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6916-96:
(6*6)+(5*9)+(4*1)+(3*6)+(2*9)+(1*6)=127
127 % 10 = 7
So 6916-96-7 is a valid CAS Registry Number.

6916-96-7Relevant academic research and scientific papers

EFFECT OF THE CHEMICAL STRUCTURE OF NITROXYL RADICALS ON THEIR REACTIVITY IN THE REACTION WITH HYDRAZOBENZENE AND TETRANITROMETHANE

Malievskii, A. D.,Koroteev, S. V.,Volodarskii, L. B.,Shapiro, A. B.

, p. 2331 - 2338 (1990)

The reaction rate constants of reduction of stable radicals of different classes by hydrazobenzene in hexane at ca. 20 deg C, in the range of 0.4 - 5*103 M-1 sec-1, were determined; a single scale of the oxidative properties of stable nitroxyl radicals was constructed.The rate constants of oxidation of a series of nitroxyl radicals by tetranitromethane in aqueous medium at ca. 20 deg C, in the range of 0.06 - 10 M-1 sec-1, were determined.It was shown that the oxidative properties of the nitroxyl group decrease slightly with an increase in its reducing properties for nitroxyl radicals of the piperidine and imidazoline series in reactions with ascorbic acid and tetranitromethane in aqueous medium, respectively.

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