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Trifluoromethyl tert-butyl nitroxide, also known as (CF3)3CNO, is a stable nitroxide radical with a trifluoromethyl group and a tert-butyl group attached to the nitrogen atom. It is a widely used spin trapping agent in electron paramagnetic resonance (EPR) spectroscopy, particularly for detecting short-lived radicals in biological and chemical systems. The molecule's stability and reactivity make it an effective tool for studying radical reactions and understanding the role of radicals in various processes. Its unique structure allows for the formation of stable nitroxide radicals upon reaction with transient radicals, which can then be analyzed using EPR techniques. Trifluoromethyl tert-butyl nitroxide is also known for its applications in materials science, as it can be used to modify polymers and improve their properties.

27695-72-3

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27695-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27695-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,9 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27695-72:
(7*2)+(6*7)+(5*6)+(4*9)+(3*5)+(2*7)+(1*2)=153
153 % 10 = 3
So 27695-72-3 is a valid CAS Registry Number.

27695-72-3Downstream Products

27695-72-3Relevant academic research and scientific papers

DARSTELLUNG UND THERMOLYSE VON HEXAKIS(PERFLUORORGANYLTHIO/SELENO)ETHANEN

Haas, Alois,Kempf, Karl W.

, p. 4963 - 4972 (2007/10/02)

Thiocarbonylcompounds such as 1a, 1b, 1c, 1d, 1e and 1f were prepared and irradiated with UV-light in hexane solution.The products obtained in this photolyses are 3a, 3b and 3c.Only 3c dissociates in the temperature range 140-190 deg C reversible to 2c.The others, 3a and 3b, decompose yielding bis(trifluoromethyl)diselenide, 6b and 6d, without forming the corresponding methyl radical 2a and 2b.This was proved by spin-trapping experiments utilizing phenyl-t-butylnitrone.Attempts to prepare 3e were unsuccessful but led to the new compounds 7a, 7b, 7c, 1,1,1-tris(trifluoromethylseleno)ethan (7d) and, surprisingly, 9.Physical and spectroscopic data of the newly prepared substances are provided.

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