88200-81-1

Basic information

• Product Name: 2,4(1H,3H)-Pyrimidinedione, 6-[(3,5-dimethylphenyl)amino]-3-methyl-
• CAS NO: 88200-81-1
• Molecular Formula: C13H15N3O2
• Molecular Weight: 245.281
• Mol File: 88200-81-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,4(1H,3H)-Pyrimidinedione, 6-[(3,5-dimethylphenyl)amino]-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 6-[(3,5-dimethylphenyl)amino]-3-methyl-(88200-81-1)
• EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 6-[(3,5-dimethylphenyl)amino]-3-methyl-(88200-81-1)

Safety Data

• Hazardous Substances Data: 88200-81-1(Hazardous Substances Data)

Upstream product

• 108-69-0 3,5-dimethylaminoaniline 
• 4318-56-3 3-methyl-6-chlorouracil 

Downstream Products

• 130806-38-1 8-(3',5'-dimethylphenyl)-3-methyl-6,7-diphenylpteridine-2,4(3H,8H)-dione 
• 130806-36-9 8-(3',5'-dimethylphenyl)-3,6,7-trimethylpteridine-2,4(3H,8H)-dione 
• 130806-34-7 8-(3',5'-dimethylphenyl)-3-methylpteridine-2,4(3H,8H)-dione 
• 130806-32-5 5-amino-6-(3,5-dimethylanilino)-3-methylpyrimidine-2,4(1H,3H)-dione 
• 117284-99-8 10-(3,5-Dimethyl-phenyl)-3-methyl-10H-benzo[g]pteridine-2,4-dione 
• 130806-30-3 6-(3,5-Dimethyl-phenylamino)-3-methyl-5-nitroso-1H-pyrimidine-2,4-dione 

Relevant articles and documents

Flavins as potential antimalarials. 2. 3-Methyl-10-(substituted-phenyl)flavins

A series of 3-methyl-10-(substituted-phenyl)flavins was prepared and tested for antimalarial activity against the lethal parasite Plasmodium vinckei in mice. Several of these analogues were found to be effective antimalarial agents. A quantitative structure-activity relationship study was undertaken with 44 analogues and no satisfactory relationship could be established.

Fluid Solution and Solid-State Electron Nuclear Double Resonance Studies of Flavin Model Compounds and Flavoenzymes

Partially deuterated and various substituted flavin and thiaflavin model compounds have been synthesized.For the first time, high-resolution H, D, and 14N ENDOR and TRIPLE resonance experiments in fluid solution have been performed on the paramagnetic derivatives of these compounds.Additionally, valuable information has been obtained about hyperfine anisotropies and molecular structures from ENDOR in rigid matrices.Solid matrix ENDOR studies of native flavoenzymes, namely, "Old Yellow Enzyme" (NADPH dehydrogenase), two flavodoxins, and a methanol oxidase are reported.The ENDOR matrix signals of the various flavoproteins are different in intensity, suggesting that the microenvironments are remarkably different.Applicabilities and limitations of the ENDOR technique in the studies of flavins and flavoenzymes are discussed.