106877-59-2 Usage
Chemical structure
A complex structure consisting of a hydantoin ring and an oxalyl moiety attached to a central benzene ring.
Application
Used in medicinal chemistry as a building block for the synthesis of potential drug candidates.
Structural features
Unique structural features that make it attractive for the development of pharmaceuticals targeting various biological pathways.
Chemical modifications
Presence of both hydantoin and oxalyl groups in the molecule provides opportunities for diverse chemical modifications to enhance its pharmacological properties.
Potential use
Utilized in the development of novel therapeutic agents for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 106877-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106877-59:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*7)+(2*5)+(1*9)=152
152 % 10 = 2
So 106877-59-2 is a valid CAS Registry Number.
106877-59-2Relevant academic research and scientific papers
REACTION OF BIS-α-DIKETONES WITH UREA IN AN ALKALINE MEDIUM
Savchenko, T. I.,Yatsimirskii, A. K.
, p. 1117 - 1122 (2007/10/02)
The condensation of bis-α-diketones C6H5COCOArCOCOC6H5 and urea with the formation of new hydantoins was investigated in an alkaline medium.The dependence of the reactivity of the bis-α-diketones on the central aryl fragment is described satisfactorily on the basis of a Hammett correlation.It was established that 1,4-di(phenyloxalyl)benzene has high sensitivity to nucleophilic attack, due to the mutal effect of the α-dicarbonyl reaction centers.From analysis of the 13C NMR and UV spectra it follows that the reactivity is probably determined not by the difference in the electron distribution at the carbons of the carbonyl groups but by their steric orientation.
