115204-73-4

Basic information

• Product Name: 9H-Purine, 2,6-dichloro-9-[(4-methylphenyl)methyl]-
• CAS NO: 115204-73-4
• Molecular Formula: C13H10Cl2N4
• Molecular Weight: 293.155
• Mol File: 115204-73-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 9H-Purine, 2,6-dichloro-9-[(4-methylphenyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Purine, 2,6-dichloro-9-[(4-methylphenyl)methyl]-(115204-73-4)
• EPA Substance Registry System: 9H-Purine, 2,6-dichloro-9-[(4-methylphenyl)methyl]-(115204-73-4)

Safety Data

• Hazardous Substances Data: 115204-73-4(Hazardous Substances Data)

Upstream product

• 106-42-3 para-xylene 
• 5451-40-1 2,6 dichloropurine 
• 104-81-4 4-Methylbenzyl bromide 

Downstream Products

• 442684-09-5 2-chloro-6-(2-furyl)-9-(4-methylphenylmethyl)-9H-purine 
• 115204-55-2 2-chloro-6-(dimethylamino)-9-(4-methylbenzyl)-9H-purine 
• 125802-42-8 6-anilino-2-chloro-9-(4-methylbenzyl)-9H-purine 

Relevant articles and documents

Metal-free, highly efficient organocatalytic amination of benzylic C-H bonds

A new synthetic approach toward direct C-N bond formation through sp 3 C-H activation has been developed under metal-free conditions. Both primary and secondary benzylic C-H substrates could react smoothly with various amines to give only mono-amination products with good to excellent yields. The Royal Society of Chemistry 2013.

Synthesis, biological activity, and SAR of antimycobacterial 9-aryl-, 9-arylsulfonyl-, and 9-benzyl-6-(2-furyl)purines

9-Aryl-, 9-arylsulfonyl- and 9-benzyl-6-(2-furyl)purines were synthesized by N-alkylation or N-arylation of the purine followed by Stille coupling to introduce the furyl substituent in the 6-position and the compounds screened for activity against Mycobac