1319212-73-1

Basic information

• Product Name: N-(but-2-yl)-2-(4,6-dichloro[1,3,5]triazin-2-ylamino)benzamide
• Synonyms: N-(but-2-yl)-2-(4,6-dichloro[1,3,5]triazin-2-ylamino)benzamide
• CAS NO: 1319212-73-1
• Molecular Weight: 340.212
• Mol File: 1319212-73-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(but-2-yl)-2-(4,6-dichloro[1,3,5]triazin-2-ylamino)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(but-2-yl)-2-(4,6-dichloro[1,3,5]triazin-2-ylamino)benzamide(1319212-73-1)
• EPA Substance Registry System: N-(but-2-yl)-2-(4,6-dichloro[1,3,5]triazin-2-ylamino)benzamide(1319212-73-1)

Safety Data

• Hazardous Substances Data: 1319212-73-1(Hazardous Substances Data)

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 30391-87-8 2-amino-N-(sec-butyl)benzamide 

Downstream Products

• 1319212-71-9 methyl 2-(4,6-bis(isobutylamino)-[1,3,5]triazin-2-ylamino)benzoate 
• 1319212-72-0 2-[4,6-bis(isobutylamino)-[1,3,5]triazin-2-ylamino]benzoic acid 
• 1319212-74-2 2-(4,6-bis(isobutylamino)-[1,3,5]triazin-2-ylamino)-N-[but-2-yl]-benzamide 

Relevant articles and documents

A facile synthesis of 6H-[1,3,5]triazino[2,1-b]quinazolin-6-ones

Triazinoquinazolinone derivatives are synthesized by cyclization of aminobenzamide-substituted triazine compounds in the presence of a proton source such as trifluoroacetic acid or hydrochloric acid. The reaction is mild, general, and gives high yield (>90%) of the cyclized product. This procedure allows, for the first time, access to triazinoquinazolinone compounds bearing different functionalities on the benzene and triazine moieties that are not available by other routes. Georg Thieme Verlag Stuttgart - New York.