285-50-7 Usage
Uses
Used in Organic Chemistry Research:
Tricyclo[5.1.0.0^3,5^]octane is utilized as a model compound for studying ring strain and reactivity in organic chemistry. Its high strain energy makes it an ideal candidate for investigating the effects of molecular strain on chemical behavior and reactions.
Used in Materials Science:
In the field of materials science, tricyclo[5.1.0.0^3,5^]octane is employed as a component in the design of molecular scaffolds. Its rigid and stable structure contributes to the development of novel materials with potential applications in various industries.
Used in Drug Discovery and Development:
Tricyclo[5.1.0.0^3,5^]octane's unusual structure and properties have been explored for potential applications in drug discovery and development. Its use in designing molecular scaffolds may lead to the creation of new pharmaceutical compounds with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 285-50-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 285-50:
(5*2)+(4*8)+(3*5)+(2*5)+(1*0)=67
67 % 10 = 7
So 285-50-7 is a valid CAS Registry Number.
285-50-7Relevant academic research and scientific papers
Electron-Transfer Reduction of Bis(gem-dihalocyclopropyl) Compounds. Evidence against the 1,4-Elimination-Type Remote Ionization of the Cyclopropylidene Radical Anion. Unusual Product Distribution as a Result of Reactions in the Region of Reagent Mixing.
Tremelling, Michael J.,Kaur, Sarjit
, p. 615 - 617 (2007/10/02)
The electron-transfer reduction of 4,4,8,8-tetrachlorotricyclo3,5>octane with a deficiency of potassium metal in an NH3/THF medium at -78 degC is reported.The only products of the reaction are starting material and the completely dechlorinated hydrocarbon, tricyclo3,5>octane.No partially reduced products containing one, two, or three chlorines were detected.These results are explained by a model in which the reaction takes place in the region of reagent mixing rather than a remote ionization effect that had previously been proposed.
