61369-42-4 Usage
Class
Pteridine derivative
Biological systems presence
Found in biological systems
Pharmacological properties
Potential antiviral, antitumor, and antifolate agents
Structural features
Methyl group and phenyl group attached to the pteridine ring
Chemical and physical properties
Unique due to the presence of the methyl and phenyl groups
Potential applications
Further research needed to fully understand its potential applications
Biological activities
May have similar biological activities as other pteridines
Research status
Further research necessary to confirm its potential applications and biological activities
Compound type
Chemical compound
Check Digit Verification of cas no
The CAS Registry Mumber 61369-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,6 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61369-42:
(7*6)+(6*1)+(5*3)+(4*6)+(3*9)+(2*4)+(1*2)=124
124 % 10 = 4
So 61369-42-4 is a valid CAS Registry Number.
61369-42-4Relevant academic research and scientific papers
Nouvelle voie d'acces aux iso-alloxazines par l'intermediaire d'alkyl-1-amino-2-tetrahydro-1,5,6,7-quinoxaline-3-carbonitriles (ou carboxylate de methyle)
Lacroix, Alain,Schabat, Dominique,Clerin, Daniel,Fleury, Jean-Pierre
, p. 1065 - 1072 (2007/10/02)
A new synthetic approach to iso-alloxazines using 1-alkyl-2-amino-1,5,6,7-tetrahydroquinoxaline-3-carbonitriles (or the corresponding methylcarboxylates) is reported.These key intermediates, accessible in two steps from cyclohexanone-enamines, when treated alkyl(aryl)iso-cyanates, guanidine or alkylchloroformates yield tetrahydro-iso-alloxazine derivatives, which can be dehydrogenated.Thus 3,10-dialkyl, 10-alkyl-3-aryl, 10-alkyl-iso-alloxazines or their 2-imino-4-oxo, 4-imino-2-oxo and 2,4-bisimino derivatives were obtained.The regiospecific aspect of this approach is illustrated by the synthesis of naphto, naphto or dimethyl-7,8 benzo pteridine derivatives.Tautomeric behavior or the tetrahydro intermediates and some limitations of the method are discussed.
