105843-07-0 Usage
Uses
Used in Pharmaceutical Industry:
3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy is used as a spin-labeled reagent for the preparation of spin-labeled analogs of biologically active compounds. This application is particularly relevant in the pharmaceutical industry, where understanding the structure and function of biologically active molecules is crucial for drug discovery and development.
Used in the Preparation of Spin-Labeled Analogs:
3-Ethenyl-2,5-dihydro-2,2,5,5-tetraMethyl-1H-pyrrol-1-yloxy is used as a spin-labeled reagent for the preparation of spin-labeled analogs of various biologically active compounds, including Morphine, Nalorphine, Barbituric acid, Choline, and Acetylcholine. These spin-labeled analogs are essential tools in studying the structure, dynamics, and interactions of these molecules, which can provide valuable insights into their biological functions and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 105843-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,4 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105843-07:
(8*1)+(7*0)+(6*5)+(5*8)+(4*4)+(3*3)+(2*0)+(1*7)=110
110 % 10 = 0
So 105843-07-0 is a valid CAS Registry Number.
105843-07-0Relevant academic research and scientific papers
Further syntheses with nitroxide &α,&β-unsaturated aldehydes and allylic bromides
Hideg, Kalman,Csekeo, Jozsef,Hankovszky, H. Olga,Sohar, Pal
, p. 1482 - 1490 (2007/10/02)
The enhanced reactivity of nitroxide allylic bromides is used for preparation of spin-labelled analogues of biologically active compounds (morphine, Nalorphine, barbituric acid, choline and acetyl choline).Nitroxide α,β-unsaturated aldehydes are reacted with phosphoranes to give nitroxide polyenes.The nitroxides are reduced to diamagnetic N-hydroxy hydrochloride salts, which can be converted in the presence of base to N-acetoxy derivatives.
