59417-51-5 Usage
Molecular structure
A complex structure consisting of a quinoxaline ring system attached to a 1,1-diphenylethanol moiety.
Quinoxaline ring
A heterocyclic aromatic ring system containing oxygen and nitrogen atoms.
Methyl group
A CH3 group attached to the quinoxaline ring at the 3-position.
1,1-Diphenylethanol moiety
A group consisting of two phenyl rings attached to a central carbon atom, which is also attached to a hydroxyl group.
Medicinal chemistry and drug development
The compound has potential biological activities that could be explored for therapeutic purposes.
Chiral auxiliary or building block
The presence of the 1,1-diphenylethanol moiety suggests potential use as a chiral auxiliary or building block for the synthesis of other complex molecules.
Further research
More investigation is needed to explore the potential applications and biological activities of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 59417-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,1 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59417-51:
(7*5)+(6*9)+(5*4)+(4*1)+(3*7)+(2*5)+(1*1)=145
145 % 10 = 5
So 59417-51-5 is a valid CAS Registry Number.
59417-51-5Relevant articles and documents
6-Lithioquinoxalines and Their Transformations
Dobrodei,El'tsov
, p. 620 - 629 (2007/10/03)
6-Bromo-2,3-diphenylquinoxaline reacts with butyllithium to give the 6-lithio derivative in a yield of more than 80%, which reacts with electrophiles such as benzophenone, Michler ketone, methyl ethyl ketone, iodine, selenium, and dimethylformamide to give the corresponding quinoxaline derivatives. 6-Bromo-2,3-dimethylquinoxaline is metallated with butyl- and phenyllithium at the methyl groups and benzene ring. These organolithium compounds react with benzophenone to give the corresponding diphenyl- and triaryl-carbinols, whose yield and ratio were determined by HPLC. These results open prospects for preparing new quinoxaline derivatives substituted at the annelated benzene ring.
