652538-76-6

Basic information

• Product Name: 3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionic acid
• Synonyms: 3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionic acid
• CAS NO: 652538-76-6
• Molecular Weight: 297.316
• Mol File: 652538-76-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionic acid(652538-76-6)
• EPA Substance Registry System: 3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionic acid(652538-76-6)

Safety Data

• Hazardous Substances Data: 652538-76-6(Hazardous Substances Data)

Upstream product

• 934524-88-6 tert-butyl 3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propanoate 
• 652538-75-5 ethyl 3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionate 
• 100-61-8 N-methylaniline 
• 54346-27-9 4-oxo-3H-pyrazolo<1,5-a>-1,3,5-triazine 
• 652539-01-0 8-iodo-4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazine 
• 652538-99-3 4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazine 

Downstream Products

• 652538-77-7 N-(4-methoxycarbonylphenyl)-3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionamide 
• 934524-82-0 N-[3-(2-oxopyrrolidin-1-yl)propyl]-3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionamide 
• 934524-83-1 N-[2-(2,2-diphenyl-1,3-benzodioxol-5-yl)ethyl]-3-[4-(N-methyl-N-phenylamino)pyrazolo[1,5-a]-1,3,5-triazin-8-yl]propionamide 
• 934524-86-4 N-[2-(2,2-diphenyl-1,3-benzodioxol-5-yl)ethyl]-3-(3,4-dihydro-4-oxopyrazolo[1,5-a]-1,3,5-triazin-8-yl)propionamide 

Relevant articles and documents

Synthesis of 8-substituted pyrazolo[1,5-a]-1,3,5-triazine derivatives by palladium-catalyzed cross-coupling reactions

8-Substituted pyrazolo[1,5-a]-1,3,5-triazine derivatives 6 were prepared from the corresponding 8-iodopyrazolo[1,5-a]-1,3,5-triazines 5 through palladium-catalyzed cross-coupling reactions. Several bioisosteres of hypoxanthine drugs 2 were then prepared b