88073-06-7 Usage
Molecular Structure
The compound has an isoindole-1,3(2H)-dione core with a 2-(1-hydroxy-2-oxo-2-phenylethyl) side chain.
Chemical Classification
It is a derivative of 1H-isoindole-1,3(2H)-dione.
Potential Pharmaceutical Properties
The compound is known for its anti-inflammatory, analgesic, antioxidant, and neuroprotective effects.
Relevance in Medicinal Chemistry
The compound is of interest for the development of new and improved drug treatments due to its unique chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 88073-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,7 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88073-06:
(7*8)+(6*8)+(5*0)+(4*7)+(3*3)+(2*0)+(1*6)=147
147 % 10 = 7
So 88073-06-7 is a valid CAS Registry Number.
88073-06-7Relevant academic research and scientific papers
Reactivity of N-Phenacyloxycarbamates and Related Systems in the Presence of Bases: Study of a New Anionic Rearrangement
Consonni, Piero,Favara, Duccio,Omodei-Sale, Amedeo,Bartolini, Giuseppe,Ricci, Alfredo
, p. 967 - 974 (2007/10/02)
N-Phenacyloxycarbamates and other systems containing a CH2-O-N= framework, in the presence of bases, undergo a CH2-O-N= -> CH(OH)-N= rearrangement.The mechanism of this reaction has been studied kinetically and through crossover and capture experiments.The bulk of the data favours an intermolecular ionic mechanism which occurs by removal of a proton from the methylene group in the rate-determining step, followed by interaction between a glyoxal molecule and a carbamate anion in the fast step of the reaction.
