1136519-32-8

Basic information

• Product Name: 8-(4-chlorophenyl)-1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione
• Synonyms: 8-(4-chlorophenyl)-1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione
• CAS NO: 1136519-32-8
• Molecular Weight: 304.736
• Mol File: 1136519-32-8.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 8-(4-chlorophenyl)-1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 8-(4-chlorophenyl)-1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione(1136519-32-8)
• EPA Substance Registry System: 8-(4-chlorophenyl)-1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione(1136519-32-8)

Safety Data

• Hazardous Substances Data: 1136519-32-8(Hazardous Substances Data)

Upstream product

• 58-08-2 3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione 
• 56075-36-6 1-(4-chlorophenyl)-2-(methylsulfonyl)diazene 
• 106-47-8 4-chloro-aniline 
• 2751-25-9 p-chlorophenylsulfonyl hydrazide 
• 14752-66-0 sodium p-chlorobenzenesulphinate 
• 1679-18-1 4-Chlorophenylboronic acid 
• 637-87-6 1-Chloro-4-iodobenzene 
• 106-39-8 bromochlorobenzene 

Relevant articles and documents

Smooth Metal-Free Photoinduced Preparation of Valuable 8-Arylxanthines

A set of 8-arylxanthines was prepared under metal-free conditions and in aqueous solvents from arylazo sulfones and caffeine or theophylline. Notably, the process took place by simply exposing the reaction vessel to visible or solar light, and unreacted xanthine could be easily recovered during the purification step.

Synthesis and characterization of amino-NHC coinage metal complexes and application for C-H activation of caffeine

This paper describes the synthesis and characterization of silver, copper and gold complexes supported by several amino-NHC ligands with different amino side arms. The transmetallation process using silver-NHC complexes can be used to prepare amino-NHC copper and gold complexes easily in high yield. In addition, the catalytic activities of copper complexes are examined for arylation of caffeine via C-H bond activation.

Palladium-catalyzed desulfitative C-H arylation of heteroarenes with sodium sulfinates

Desulfitative C-H arylation: Palladium-catalyzed desulfitative C-H arylation of heteroarenes with sodium sulfinates has been disclosed to construct aryl-heteroaryl bonds without the need for any extra ligands (see scheme). Copyright