73586-31-9 Usage
Appearance
Colorless, odorless liquid at room temperature and pressure
Structure
Bicyclic hydrocarbon compound
Isomerization
Can rapidly and reversibly isomerize to its corresponding isomer, norbornadiene, upon exposure to light or heat
Applications
+ Molecular switches
+ Solar thermal fuels
+ Energy storage systems
+ Chemical intermediate in the synthesis of various organic compounds
Unique properties
Quadricyclane exhibits potential as a chemical intermediate due to its unique structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 73586-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,8 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73586-31:
(7*7)+(6*3)+(5*5)+(4*8)+(3*6)+(2*3)+(1*1)=149
149 % 10 = 9
So 73586-31-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14/c1-6-2-8-4-7(1)10-5-11(8,10)9(10)3-6/h6-9H,1-5H2
73586-31-9Relevant academic research and scientific papers
Intramolecular γ C-H Insertion vs. Olefin Cycloaddition in 4-Methylene-2-adamantylidene and 8-Methylene-2-noradamantylidene
Majerski, Zdenko,Hamersak, Zdenko,Mlinaric-Majerski, Katica
, p. 1830 - 1831 (2007/10/02)
8-Methylene-2-noradamantylidene inserts readily into γ C-H bond giving 6-methylene-2,4-didehydro-noradamantane rather than the olefin-cycloaddition product, while its higher homologue 4-methylene-2-adamanthylidene reacts exclusively by intramolecular cycloaddition to the olefinic bond yielding 2,4-methano-2,4-didehydroadamantane, a propellane.
