922500-97-8 Usage
Uses
Used in Polymer Production:
3,3-diMethoxyoxetane is used as a monomer for the production of polymers, contributing to the creation of materials with specific properties required in different applications.
Used in Pharmaceutical and Agrochemical Synthesis:
In the pharmaceutical and agrochemical industries, 3,3-diMethoxyoxetane is utilized as a component in the synthesis of various compounds, playing a crucial role in the development of new drugs and agrochemical products.
Used as a High-Energy Fuel Additive:
3,3-diMethoxyoxetane is studied for its potential use as a high-energy fuel additive due to its high energy density, which can improve the performance and efficiency of fuels.
Used in Material Development:
3,3-diMethoxyoxetane is also investigated for its use in the development of new materials, where its unique properties can contribute to the advancement of material sciences.
Used as a Reagent in Organic Chemistry Reactions:
3,3-diMethoxyoxetane serves as a reagent in various organic chemistry reactions, facilitating specific chemical transformations and synthesis processes.
Check Digit Verification of cas no
The CAS Registry Mumber 922500-97-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,5,0 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 922500-97:
(8*9)+(7*2)+(6*2)+(5*5)+(4*0)+(3*0)+(2*9)+(1*7)=148
148 % 10 = 8
So 922500-97-8 is a valid CAS Registry Number.
922500-97-8Relevant academic research and scientific papers
Wuitschik, Georg,Rogers-Evans, Mark,Mueller, Klaus,Fischer, Holger,Wagner, Bjoern,Schuler, Franz,Polonchuk, Liudmila,Carreira, Erick M.
, p. 7736 - 7739 (2006)
(Chemical Equation Presented) Ring the changes: Introduction of an oxetane ring results in remarkably improved physico- and biochemical properties of the underlying scaffold. The oxetane ring confers enhanced solubility, reduces the metabolic degredation, lipophilicity, and amphiphilicity, and modulates the basicity of a nearby amine group.
