1036-65-3

Basic information

• Product Name: 1H-Pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione, 6-(4-methoxyphenyl)-1,3-dimethyl-
• CAS NO: 1036-65-3
• Molecular Formula: C15H15N3O3
• Molecular Weight: 285.302
• Mol File: 1036-65-3.mol

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione, 6-(4-methoxyphenyl)-1,3-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione, 6-(4-methoxyphenyl)-1,3-dimethyl-(1036-65-3)
• EPA Substance Registry System: 1H-Pyrrolo[3,2-d]pyrimidine-2,4(3H,5H)-dione, 6-(4-methoxyphenyl)-1,3-dimethyl-(1036-65-3)

Safety Data

• Hazardous Substances Data: 1036-65-3(Hazardous Substances Data)

Usage

Chemical class

pyrimidine and pyrrolopyrimidine
A heterocyclic compound with a pyrrolopyrimidine core structure.

Core structure

pyrrolopyrimidine
The compound is based on a core structure that consists of a pyrrole and a pyrimidine ring fused together.

Substituents

1,3-dimethyl
Two methyl groups are attached to the 1 and 3 positions of the pyrrolopyrimidine core, contributing to its structure.

Additional group

6-(4-methoxyphenyl)
A 4-methoxyphenyl group is attached to the 6th position of the pyrrolopyrimidine core, which influences its properties and reactivity.

Potential applications

pharmaceutical research and drug development
The compound has potential biological activities and medicinal properties, making it a candidate for further studies in drug development.

Need for further research

yes
More studies and research are needed to fully understand and explore the potential uses and applications of this chemical compound.

Upstream product

• 85102-48-3 5-Hydroxy-6-(4-methoxy-phenyl)-1,3-dimethyl-1,5-dihydro-pyrrolo[3,2-d]pyrimidine-2,4-dione 
• 741-86-6 6-(4-methoxy-styryl)-1,3-dimethyl-5-nitro-1H-pyrimidine-2,4-dione 
• 123-11-5 4-methoxy-benzaldehyde 
• 104-82-5 4-Methylbenzyl chloride 
• 85102-52-9 1,3-Dimethyl-5-nitro-6-(2-p-tolyl-ethyl)-1H-pyrimidine-2,4-dione 
• 55326-07-3 1,3,6-trimethyl-5-nitrouracil 

Relevant articles and documents

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

Syntheses of 9-Deazatheophyllines and 6-Deoxy-9-deazatheophyllines

The reaction of 1,3-dimethyl-5-nitro-6-styryluracils (IIa-e) with sodium dithionite in formic acid afforded the corresponding 8-aryl-9-deazatheophyllines (IVa-e).The reaction of IVa with phosphorus oxychloride gave 6-chloro-6-deoxy-8-phenyl-9-deazatheophy