75427-52-0

Basic information

• Product Name: Pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione, 8-hydroxy-3,10-dimethyl-
• CAS NO: 75427-52-0
• Molecular Formula: C13H11N3O3
• Molecular Weight: 257.249
• Mol File: 75427-52-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione, 8-hydroxy-3,10-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione, 8-hydroxy-3,10-dimethyl-(75427-52-0)
• EPA Substance Registry System: Pyrimido[4,5-b]quinoline-2,4(3H,10H)-dione, 8-hydroxy-3,10-dimethyl-(75427-52-0)

Safety Data

• Hazardous Substances Data: 75427-52-0(Hazardous Substances Data)

Upstream product

• 591-27-5 m-Hydroxyaniline 
• 123-08-0 4-hydroxy-benzaldehyde 
• 5759-63-7 6-methylamino-3-methyluracil 
• 14703-69-6 3-(N-methylamino)phenol 
• 59997-20-5 6-chloro-3-methyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde 
• 22532-60-1 2-bromo-4-hydroxybenzaldehyde 
• 56962-11-9 2-chloro-4-hydroxybenzaldehyde 
• 76837-69-9 6-(3-Hydroxy-N-methyl-anilino)-3-methyl-2,4(1H,3H)-pyrimidindion 
• 68-12-2 N,N-dimethyl-formamide 
• 75427-41-7 C₁₉H₂₂N₆O₅ 

Relevant articles and documents

The autorecycling oxidation of benzylamine by synthetic 8-hydroxy-5-deazaflavin derivatives

Various 8-hydroxy-5-deazaflavin derivatives were synthesized as the model compounds of coenzyme F420. These compounds oxidized benzylamine to benzaldehyde more efficiently than the corresponding 8-unsubstituted 5-deazaflavin.

A New, General, and Convenient Synthesis of 5-Deazaflavins (5-Deazaisoallooxazines)

The condensation of 6-substituted-aminouracils with o-halogenobenzaldehydes in dimethylformamide led to the formation of the corresponding 5-deazaflavins in a single step.

Donator-substituted 5-Deazaflavins, II: Hydroxy- and 8-Dimethylamino-5-deazaflavins - Model Compounds of Naturally Occuring (Deaza-)Flavocoenzyms

Donator-substituted 5-deazaflavins 7 were prepared by a Vilsmeier procedure from the anilinouracil derivatives 5 via 6 as stable intermediates.Spectroscopic comparison of the 5-deazaflavins 7 shows, that resonance of the substituents increases in the sequ