112422-85-2 Usage
Structure
Cyclobutane ring with two phenyl groups attached to the 1 and 3 positions
Type of Compound
Cyclic compound
Rigidity
Rigid structure
Usage
Often used in organic synthesis and as a building block for creating more complex molecules
Presence of Phenyl Groups
Makes the compound useful in the development of new materials and pharmaceuticals
Potential Applications
Drug discovery and materials science
Unique Structure
Contributes to its potential in various fields
Check Digit Verification of cas no
The CAS Registry Mumber 112422-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,2 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112422-85:
(8*1)+(7*1)+(6*2)+(5*4)+(4*2)+(3*2)+(2*8)+(1*5)=82
82 % 10 = 2
So 112422-85-2 is a valid CAS Registry Number.
112422-85-2Relevant academic research and scientific papers
CYCLOBUTANEDIYLS: A NEW CLASS OF LOCALIZED BIRADICALS. SYNTHESIS AND EPR SPECTROSCOPY.
Jain,Sponsler,Coms,Dougherty
, p. 1356 - 1366 (2007/10/11)
Nine triplet cyclobutanediyls (1) have been synthesized and observed by matrix isolation EPR spectroscopy. The zero-field splitting (zfs) parameters provide detailed information on the spin densities in these structures. The observed zfs values can be quantitatively modeled by using a straightforward semiempirical scheme, as long as one explicitly incorporates the spin polarization effects known to be important in radicals such as allyl and benzyl. In addition, interpretable hyperfine coupling (hfc) has been observed in many cyclobutanediyls. Spectral simulation produces the hfc constants, which provide further information on spin distribution and indicate that the four-membered ring in 1 is planar.
