226247-80-9

Basic information

• Product Name: 9H-Purin-2-amine, 9-(phenylmethyl)-
• CAS NO: 226247-80-9
• Molecular Formula: C12H11N5
• Molecular Weight: 225.253
• Mol File: 226247-80-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 9H-Purin-2-amine, 9-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Purin-2-amine, 9-(phenylmethyl)-(226247-80-9)
• EPA Substance Registry System: 9H-Purin-2-amine, 9-(phenylmethyl)-(226247-80-9)

Safety Data

• Hazardous Substances Data: 226247-80-9(Hazardous Substances Data)

Upstream product

• 6336-42-1 2-amino-9-benzyl-6-chloro-9H-purine 
• 611-19-8 1-chloro-2-(chloromethyl)benzene 
• 452-06-2 7H-purin-2-amine 
• 1526929-38-3 C₁₂H₁₃N₇ 
• 68462-61-3 ethyl 5‐amino‐1‐benzyl‐1H‐imidazole‐4‐carboxylate 
• 228263-00-1 9-benzyl-2,6-bis(ethoxycarbonyl)purine 
• 228262-99-5 5-amino-1-benzyl-4-imidazolecarboxylic acid 
• 934001-77-1 9-benzyl-2-(ethoxycarbonyl)purine 
• 934001-78-2 9-benzyl-2-(hydrazinocarbonyl)purine 

Downstream Products

• 943753-40-0 2-amino-8-cyano-9-benzylpurine 
• 1197007-77-4 C₁₉H₁₇N₅ 
• 226247-84-3 9-benzyl-2-ethenyl-9H-purine 
• 624738-27-8 9-benzyl-8-bromo-9H-purine-2-amine 
• 226247-82-1 9-benzyl-2-iodo-9H-purine 

Relevant articles and documents

The synthesis of nebularine and its analogs via oxidative desulfuration in aqueous nitric acid

The synthesis of nebularine and its analogs has been achieved via oxidative desulfuration in H2O for the first time. With 50% HNO3as an oxidant and solvent, 18 products were obtained in good yields (70%–94%). The oxidative desulfuration system could tolerate different functional groups including fluoro, chloro, amino, alkyl, allyl, ribosyl, deoxyribosyl, and arabinofuranosyl groups.More importantly, the drug nebularine could be obtained successfully on a 20 g scale, which made this route more attractive for industrial applications.

A site selective C-H arylation of free-(NH2) adenines with aryl chlorides: Application to the synthesis of 6,8-disubstituted adenines

An efficient site selective method for the direct arylation of free-(NH2) adenines 1 to provide a range of C-8 arylated adenines 3 in excellent yields is described. This process based on the use of Pd(OH) 2/C as the catalyst and a st

Addition and Cycloaddition to 2- and 8-Vinylpurines

The reactivity of purines carrying an alkenyl substituent in the 2- or 8-position in nucleophilic addition and cycloaddition reactions has been studied. A vinyl substituent situated at C-8 is highly electrophilic and readily participates as a Michael acce