61369-41-3

Basic information

• Product Name: 10-(2-methoxyethyl)-3-phenyl-6,8,9,10-tetrahydrobenzo[g]pteridine-2,4(3H,7H)-dione
• CAS NO: 61369-41-3
• Molecular Formula: C₁₉H₂₀N₄O₃
• Molecular Weight: 352.3871
• Mol File: 61369-41-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 500.4°C at 760 mmHg
• Flash Point: 256.4°C
• Density: 1.37g/cm³
• Vapor Pressure: 3.82E-10mmHg at 25°C
• Refractive Index: 1.682
• CAS DataBase Reference: 10-(2-methoxyethyl)-3-phenyl-6,8,9,10-tetrahydrobenzo[g]pteridine-2,4(3H,7H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 10-(2-methoxyethyl)-3-phenyl-6,8,9,10-tetrahydrobenzo[g]pteridine-2,4(3H,7H)-dione(61369-41-3)
• EPA Substance Registry System: 10-(2-methoxyethyl)-3-phenyl-6,8,9,10-tetrahydrobenzo[g]pteridine-2,4(3H,7H)-dione(61369-41-3)

Safety Data

• Hazardous Substances Data: 61369-41-3(Hazardous Substances Data)

Usage

Category

Pteridine derivatives

Structure

Complex, containing a pteridine ring fused with a benzene ring, a phenyl group, and a 2-methoxyethyl group

Synthesis

Produced through a series of chemical reactions

Applications

Used in research and industrial applications

Potential Properties

May have pharmaceutical properties

Biological Activities

Could be studied for its biological activities and therapeutic potentials

Further Research

Additional research and testing are necessary to fully understand the potential uses and effects of this compound

Safety

Unknown; caution should be exercised when handling due to its complex structure and potential pharmaceutical properties

Upstream product

• 61369-37-7 3-amino-4-(2-methoxy-ethyl)-4,6,7,8-tetrahydro-quinoxaline-2-carboxylic acid methyl ester 
• 103-71-9 phenyl isocyanate 
• 61369-39-9 (methoxy-2-ethyl)-1-(phenylcarbamoyl)imino-2-hexahydro-1,2,5,6,7,8-quinoxalinecarboxylate-3 de methyle 

Downstream Products

• 61369-43-5 (methoxy-2-ethyl)-10-phenyl-3-iso-alloxazine 

Relevant articles and documents

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)

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.