1269527-19-6

Basic information

• Product Name: N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine
• Synonyms: N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine
• CAS NO: 1269527-19-6
• Molecular Weight: 397.891
• Mol File: 1269527-19-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine(1269527-19-6)
• EPA Substance Registry System: N₂-(4-chlorophenyl)-6-((5-methyl-1H-benzo[d]imidazol-2-ylthio)methyl)-1,3,5-triazine-2,4-diamine(1269527-19-6)

Safety Data

• Hazardous Substances Data: 1269527-19-6(Hazardous Substances Data)

Upstream product

• 30355-61-4 6-(chloromethyl)-N²-(4-chlorophenyl)-1,3,5-triazine-2,4-diamine 
• 27231-36-3 5-methyl-2-benz-1,3-imidazoline-2-thione 
• 4022-81-5 1-(4-chlorophenyl)biguanide hydrochloride 
• 106-47-8 4-chloro-aniline 
• 496-72-0 4-methyl-1,2-diaminobenzene 

Relevant articles and documents

Synthesis and antiviral activity of benzimidazolyl-and triazolyl-1,3,5- triazines

A novel series of 1,3,5-triazine analogs was successfully synthesized through conjugation with benzimidazole or 1,2,4-triazole derivatives via a methylenethio linker. The new analogs were in vitro evaluated against HSV-1 in Vero cells; among these analogs, two compounds exhibited good effect in inhibiting HSV-1 replication (for compound 5p: EC50 = 3.5 μg/ml, SI = 358; for compound 5r: EC50 = 5.0 μg/ml, SI = 300) in comparison to acyclovir. Springer Science+Business Media, LLC 2011.