5114-94-3 Usage
Molecular structure
1-Piperidinyloxy, 4,4',4''-[1,3,5-benzenetriyltris(carbonyloxy)]tris[2,2,6,6-tetramethylis a nitroxide radical with a unique molecular structure that includes a piperidine ring, a benzene ring, and multiple carbonyloxy and methyl groups.
Stability
This compound is a stable nitroxide radical, meaning it does not easily undergo chemical reactions or decomposition.
Use as a spin-label
The compound is commonly used as a spin-label in EPR (electron paramagnetic resonance) spectroscopy, which is a technique used to study the structure and dynamics of molecules.
Use as a polymerization inhibitor
The compound can be used as a polymerization inhibitor, which helps to prevent the undesired polymerization of monomers in chemical reactions.
Use as a radical scavenger
The compound can also act as a radical scavenger, which means it can neutralize free radicals and prevent them from causing damage in chemical reactions.
Potential applications in organic synthesis
The compound has potential applications in the field of organic synthesis due to its unique molecular structure and reactivity.
Use as a stabilizer in polymer production
The compound can be used as a stabilizer in the production of polymers, which helps to prevent the degradation of the polymers during processing.
Study and manipulation of radical species
The compound's unique molecular structure and stability make it a valuable tool in the study and manipulation of radical species in various chemical and biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 5114-94-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5114-94:
(6*5)+(5*1)+(4*1)+(3*4)+(2*9)+(1*4)=73
73 % 10 = 3
So 5114-94-3 is a valid CAS Registry Number.
5114-94-3Relevant articles and documents
Directing the pathway of orthogonal 'click' reactions by modulating copper-catalytic activity
Jia, Zhongfan,Bell, Craig A.,Monteiro, Michael J.
, p. 4165 - 4167 (2011)
Control of the rates of orthogonal 'click' reactions in one pot allowed the design of highly branched macromolecular architectures. Construction of these architectures via a divergent, convergent or parallel sequence was modulated by the copper catalyst a
