163020-64-2

Basic information

• Product Name: 2-(3,5-dichloroanilino)-6-chloro-9-<<1,3-bis(benzyloxy)-2-propoxy>methyl>purine
• Synonyms: 2-(3,5-dichloroanilino)-6-chloro-9-<<1,3-bis(benzyloxy)-2-propoxy>methyl>purine
• CAS NO: 163020-64-2
• Molecular Weight: 598.916
• Mol File: 163020-64-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(3,5-dichloroanilino)-6-chloro-9-<<1,3-bis(benzyloxy)-2-propoxy>methyl>purine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,5-dichloroanilino)-6-chloro-9-<<1,3-bis(benzyloxy)-2-propoxy>methyl>purine(163020-64-2)
• EPA Substance Registry System: 2-(3,5-dichloroanilino)-6-chloro-9-<<1,3-bis(benzyloxy)-2-propoxy>methyl>purine(163020-64-2)

Safety Data

• Hazardous Substances Data: 163020-64-2(Hazardous Substances Data)

Upstream product

• 163020-53-9 2-(N-formyl-3,5-dichloroanilino)-6-chloropurine 
• 74564-16-2 1,3-dibenzyloxy-2-(chloromethoxy)propane 
• 163020-52-8 2-(3,5-dichloroanilino)-6-chloropurine 

Downstream Products

• 163020-81-3 N²-(3,5-dichlorophenyl)-9-<<1,3-bis(benzyloxy)-2-propoxy>methyl>guanine 
• 163020-82-4 N²-(3,5-dichlorophenyl)-9-<<1,3-bis(benzyloxy)-2-propoxy>methyl>adenine 

Relevant articles and documents

Haloanilino derivatives of pyrimidines, purines, and purine nucleoside analogs: Synthesis and activity against human cytomegalovirus

2-Anilinopurines and 6-anilinopyrimidines bearing 3,4- or 3,5-dichloro substituents in the anilino ring inhibited virus-specific DNA synthesis by human cytomegalovirus (HCMV)-infected human embryonic lung (HEL) cells in culture. In general, active compounds had moderate to low selectivity for viral vs host cell DNA synthesis. Nucleoside and acyclonucleoside analogs of 2-(3,5-dichloroanilino)purines inhibited both HCMV and cellular DNA synthesis at similar concentrations. 2-Amino-4-chloro-6-(3,5- dichloroanilino)pyrimidine and several related compounds inhibited HCMV growth in yield reduction assays at concentrations that were nontoxic to HEL cells.