57196-70-0

Basic information

• Product Name: 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-(4-methylphenyl)-
• CAS NO: 57196-70-0
• Molecular Formula: C14H14N4O2
• Molecular Weight: 270.291
• Mol File: 57196-70-0.mol

Chemical Properties

• CAS DataBase Reference: 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-(4-methylphenyl)-(57196-70-0)
• EPA Substance Registry System: 1H-Purine-2,6-dione, 3,7-dihydro-1,3-dimethyl-8-(4-methylphenyl)-(57196-70-0)

Safety Data

• Hazardous Substances Data: 57196-70-0(Hazardous Substances Data)

Upstream product

• 65627-03-4 4-methyl-benzaldehyde (1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-hydrazone 
• 1203-25-4 6-chloro-1,3-dimethyl-5-nitrouracil 
• 104-87-0 4-methyl-benzaldehyde 
• 1972-28-7 diethylazodicarboxylate 
• 5440-00-6 4,5-Diamino-1,3-dimethyluracil 
• 99-94-5 p-Toluic acid 
• 104-84-7 para-methylbenzylamine 
• 20886-66-2 6-amino-1,3-dimethyl-5-(4-methyl-benzylideneamino)-1H-pyrimidine-2,4-dione 
• 90994-71-1 1,3-Dimethyl-6-(4-methyl-benzylamino)-5-nitro-1H-pyrimidine-2,4-dione 

Relevant articles and documents

Exploration of polystyrene-supported 2-isobutoxy-1-isobutoxycarbonyl-1,2- dihydroquinoline (PS-IIDQ) as new coupling agent for the synthesis of 8-substituted xanthine derivatives

Polystyrene-supported 2-isobutoxy-1-isobutoxycarbonyl-1,2-dihydroquinoline (PS-IIDQ), a polymer supported covalent coupling reagent, was successfully employed for the first time in the synthesis of 8-substituted xanthine derivatives. PS-IIDQ was observed

A mild method for the preparation of 8-substituted xanthines from 5,6- diaminouracils

The Schiff base derivatives (3), prepared from the respective 5,6- diaminouracil (1) and aldehydes can be mildly oxidatively cyclized with m- CPBA in MeCN to afford C-8 substituted xanthines (6).

Synthesis and in vitro bronchospasmolytic activity of 8-aryl, heteroaryl or arylalkyl theophyllines

Twenty-four 8-aryl- or 8-heteroaryl-substituted theophyllines have been synthesized.The substituents are aromatic rings and heterocycles likely to induce an antiallergic effect or a spasmolytic activity.In vitro evaluation of the bronchospasm caused by ac

Reaction of 6-Arylidenehydrazino-1,3-dimethyluracils with Thionyl Chloride Leading to Purine, Thiazolopyrimidine, Pyrimidothiadiazine, Pyrazolopyrimidine, and Thiadiazolopyrimidine Derivatives

The reaction of 6-arylidenehydrazino-1,3-dimethyluracils with thionyl chloride in benzene afforded purine, thiazolopyrimidine, pyrimidothiadiazine, pyrazolopyrimidine, and thiadiazolopyrimidine derivatives, while

Pyrimidine Derivatives and Related Compounds. Part 47. A New Synthesis of Xanthines and Pyrrolopyrimidines by Intramolecular Cyclisation of 6-Substituted 5-Nitrouracil Derivatives

6-Arylalkylamino-1,3-dimethyl-5-nitrouracils (2a-f) were prepared by reaction of 6-chloro-1,3-dimethyl-5-nitrouracil (1) with arylalkylamines in the presence of triethylamine.Among them, the 6-arylalkylaminouracils (2a-d), possessing no substituent at the