62196-39-8

Basic information

• Product Name: 9H-Purine-6-carbonitrile, 9-phenyl-
• CAS NO: 62196-39-8
• Molecular Formula: C12H7N5
• Molecular Weight: 221.221
• Mol File: 62196-39-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 9H-Purine-6-carbonitrile, 9-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Purine-6-carbonitrile, 9-phenyl-(62196-39-8)
• EPA Substance Registry System: 9H-Purine-6-carbonitrile, 9-phenyl-(62196-39-8)

Safety Data

• Hazardous Substances Data: 62196-39-8(Hazardous Substances Data)

Upstream product

• 5470-24-6 6-Chloro-9-phenyl-9H-purine 
• 151-50-8 potassium cyanide 
• 116943-97-6 1-benzoyl-1,6-dihydro-9-phenyl-9H-purine-6-carbonitrile 
• 62141-41-7 6-(p-toluenesulfonyl)-9-phenyl-9H-purine 
• 119980-74-4 6-iodo-9-phenyl-9H-purine 

Downstream Products

• 85107-06-8 9-phenyl-6-(1-piperidinecarboximidoyl)9H-purne 
• 85107-13-7 methyl 5-amino-6-anilino-4-pyrimidinecarboxylate 
• 85107-12-6 9-phenyl-9H-purine-6-carboxamide 
• 85107-10-4 methyl 9-phenyl-9H-purine-6-carboxylate 
• 85107-07-9 6-acetyl-9-phenyl-9H-purine 
• 85107-14-8 5-Amino-6-phenylamino-pyrimidine-4-carboxylic acid ethyl ester 
• 85107-11-5 9-Phenyl-9H-purine-6-carboxylic acid ethyl ester 
• 85107-08-0 1-(9-Phenyl-9H-purin-6-yl)-propan-1-one 
• 85107-09-1 phenyl(9-phenyl-9H-purin-6-yl)methanone 
• 85107-04-6 9-phenyl-9H-purine-6-carboxamidorazone 
• 85107-03-5 9-phenyl-9H-purine-6-carboxamidoxime 
• 85107-05-7 N-butyl-9-phenyl-9H-purine-6-carboxamidine 
• 134440-73-6 5-(Diethylamino)-6-methyl-3-phenyl-3H-imidazo<4,5-b><1,5>diazocine-9-carbonitrile 
• 85107-18-2 9-phenyl-9H-purine-6-carbohydraziden 

Relevant articles and documents

Preparation of Heteroarenecarbonitriles by Reaction of Haloheteroarenes with Potassium Cyanide Catalyzed by Sodium p-Toluenesulfinate

Several heteroarenecarbonitriles were prepared by reaction of haloheteroarenes with potassium cyanide catalyzed by sodium p-toluenesulfinate (1) or sodium methanesulfinate (2).In the reaction pathway, the cyanation proceeds through the formation of the su

Purines. VIII. Reactions of 1-Benzoyl-1,6-dihydro-9-phenyl-9H-purine-6-carbonitrile (9-Phenylpurine Reissert Compound) with Acid, Bases, and Electrophiles

1-Benzoyl-1,6-dihydro-9-phenyl-9H-purine-6-carbonitrile (1, 9-phenylpurine Reissert compound) was hydrolyzed in an acid medium to give the ring fission product of the pyrimidine ring (3, 4).Alkaline hydrolysis of 1 gave 9-phenyl-9H-purine (2) and benzoic acid (5).The anion of 1 generated from 1 and sodium hydride in tetrahydrofuran underwent aromatization, resulting in the formation of 9-phenyl-9H-purine-6-carbonitrile (6) together with 2.The reaction of 1 with aromatic aldehydes in the presence of sodium hydride proceeded to give the 6-purinylmethyl benzoates (8a-c), together with 2 and 9.On the other hand, the reaction of 1 with 2,4-dinitrochlorobenzene in the presence of sodium hydride failed to give the corresponding 6-arylpurine, and the aromatization product 6 was obtained.Keywords - 9H-purine; Reissert compound anion; 9H-purin-6-ylmethyl benzoate