192447-61-3

Basic information

• Product Name: 4-Pyridinamine, 2,6-dibromo-N-methyl-N-(phenylmethyl)-
• CAS NO: 192447-61-3
• Molecular Formula: C13H12Br2N2
• Molecular Weight: 356.06
• Mol File: 192447-61-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-Pyridinamine, 2,6-dibromo-N-methyl-N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pyridinamine, 2,6-dibromo-N-methyl-N-(phenylmethyl)-(192447-61-3)
• EPA Substance Registry System: 4-Pyridinamine, 2,6-dibromo-N-methyl-N-(phenylmethyl)-(192447-61-3)

Safety Data

• Hazardous Substances Data: 192447-61-3(Hazardous Substances Data)

Upstream product

• 193074-42-9 (2,6-dibromo-4-pyridin-4-yl)-methylamine 
• 100-39-0 benzyl bromide 
• 68-12-2 N,N-dimethyl-formamide 
• 98027-81-7 2,6-dibromo-4-nitro-pyridine 1-oxide 
• 103-67-3 benzyl-methyl-amine 
• 175422-04-5 2,6-dibromo-4-nitropyridine 

Downstream Products

• 192447-52-2 2-bromo-4-{methyl(phenylmethyl)-amino}-6-{3-(trifluoromethyl)phenoxy} pyridine 

Relevant articles and documents

Regioselective synthesis of 2,4,6-triaminopyridines

A regioselective synthesis of 2,4,6-trisubstituted pyridine is described starting from 2,6-dibromo-4-nitropyridine. All three different regioisomers of the 2,4,6-triamino substituted pyridine have been synthesized in four to five steps. The method described is a general route to unsymmetrical 2,4,6-trisubstituted amino pyridines.

Process for producing pyridinecarboxamides or thiocarboxamides

A process for producing N-substituted pyridine carboxamide or thiocarboxamide, comprising reacting a substituted or unsubstituted pyridine metal compound with substituted isocyanate or isothiocyanate to obtain an addition reaction product thereof, and then substituting the metal of said addition reaction product with a proton. The process according to the present invention can be applied even to compounds having an oxidation-susceptible substituent group and, therefore, industrially useful.