863677-59-2

Basic information

• Product Name: 2-Pyridinamine, N-[2,6-bis(1-methylethyl)phenyl]-
• CAS NO: 863677-59-2
• Molecular Formula: C17H22N2
• Molecular Weight: 254.375
• Mol File: 863677-59-2.mol

Chemical Properties

• CAS DataBase Reference: 2-Pyridinamine, N-[2,6-bis(1-methylethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyridinamine, N-[2,6-bis(1-methylethyl)phenyl]-(863677-59-2)
• EPA Substance Registry System: 2-Pyridinamine, N-[2,6-bis(1-methylethyl)phenyl]-(863677-59-2)

Safety Data

• Hazardous Substances Data: 863677-59-2(Hazardous Substances Data)

Upstream product

• 109-04-6 2-bromo-pyridine 
• 24544-04-5 2,6-diisopropylbenzenamine 
• 504-29-0 2-aminopyridine 
• 163704-47-0 2-iodo-1,3-diisopropylbenzene 
• 1628-89-3 2-methoxypyridine 

Downstream Products

• 929296-32-2 [bis((2,6-diisopropylphenyl)(pyridin-2-yl)amide)tris(benzyl)tantalum] 
• 914480-32-3 [trichlorobis((2,6-diisopropylphenyl)(pyridin-2-yl)amide)tantalum] 
• 1330629-41-8 [(1,2,3,4,5-pentamethylcyclopentadienyl)Hf(N-(2,6-diisopropylphenyl)pyridine-2-amido)Me₂] 
• 1291099-50-7 N-(2,6-diisopropyl)phenyl-N-(2-pyridyl)-N-(2-quinolyl)amine 
• 1155271-57-0 [Ti(2-[(2,6-diisopropylphenyl)amino]pyridinate)3] 

Relevant articles and documents

CuI/2-Aminopyridine 1-Oxide Catalyzed Amination of Aryl Chlorides with Aliphatic Amines

A class of 2-aminopyridine 1-oxides are discovered to be effective ligands for the Cu-catalyzed amination of less reactive (hetero)aryl chlorides. A wide range of functionalized (hetero)aryl chlorides reacted with various aliphatic amines to afford the desired products in good to excellent yields under the catalyst of CuI/2-aminopyridine 1-oxides. Furthermore, the catalyst system worked well for the coupling of cyclic secondary amines and N-methyl benzylamine with (hetero)aryl chlorides.

Anticancer-Active N-Heteroaryl Amines Syntheses: Nucleophilic Amination of N-Heteroaryl Alkyl Ethers with Amines

A mild amination protocol of N-heteroaryl alkyl ethers with various amines is described. This transformation is achieved by utilizing simple and readily available base as promoter via C-O bond cleavage, offering a new amination strategy to access several anticancer-active compounds. This work is highlighted by the excellent functional group compatibility, scalability, wide substrate scope, and easy derivatization of a variety of drugs.

Pentamethylcyclopentadienyltitanium aryl(pyridyl)amide complexes: Synthesis, characterization and catalytic performance for olefin polymerization

A series of new half-sandwich pentamethylcyclopentadienyl titanium (IV) aryl(pyridyl)amide complexes, Cp?TiCl2[N(Ar)(2-Py)] [Ar = 2,6-iPr2Ph (1), 2,6-Et2Ph (2), 2,6-Me2Ph (3), 4-MePh (4)], have been s

Nucleophilic Difluoroalkylation of Isocyanates with Difluoromethyl 2-Pyridyl Sulfone

The nucleophilic difluoroalkylation of isocyanates with difluoromethyl 2-pyridyl sulfone furnished 2,2-difluoro-2-pyridinylsulfonylacetamides with good to excellent yield. These products can be converted to 2,2-difluoroacetamide sulfinate, iododifluoroacetamide and 2-aminopyridine derivatives easily.

Synthesis and structure of trialkyltantalum complexes stabilized by aminopyridinato ligands

(4-Methylpyridin-2-yl)(trimethylsilyl)amine (1), (6-methylpyridin-2-yl) (trimethylsilyl)amine (2), and (2,6-diisopropylphenyl)(pyridin-2-yl)ainine (3) were deprotonated and used as ligands to synthesize trialkyltantalum complexes. The reaction of 2 equiv.