1333119-98-4

Basic information

• Product Name: C₁₂H₁₅NO₂
• Synonyms: C₁₂H₁₅NO₂
• CAS NO: 1333119-98-4
• Molecular Weight: 205.257
• Mol File: 1333119-98-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₂H₁₅NO₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₂H₁₅NO₂(1333119-98-4)
• EPA Substance Registry System: C₁₂H₁₅NO₂(1333119-98-4)

Safety Data

• Hazardous Substances Data: 1333119-98-4(Hazardous Substances Data)

Upstream product

• 88166-78-3 1-(2,5-dimethylphenyl)ethanone oxime 
• 108-24-7 acetic anhydride 

Downstream Products

• 1333120-03-8 2,6-bis(2,5-dimethylphenyl)-4-phenylpyridine 
• 881040-60-4 2-(2,5-dimethylphenyl)imidazo[1,2-a]pyridine 

Relevant articles and documents

Copper-Catalyzed coupling of oxime acetates with aldehydes: A new strategy for synthesis of pyridines

Copper-catalyzed coupling of oxime acetates with aldehydes offers a new strategy for the synthesis of highly substituted pyridines. This novel method tolerates a wide range of functionality and allows for rapid elaboration of the oxime acetates into a variety of substituted pyridines.

Iron-Catalyzed Cyclization of Ketoxime Carboxylates and Tertiary Anilines for the Synthesis of Pyridines

A novel and efficient iron-catalyzed cyclization of ketoxime carboxylates and N,N-dialkylanilines for the modular synthesis of diverse pyridines was developed. The reaction was initiated by Fe-catalyzed N-O bond cleavage of ketoxime carboxylates in the presence of tertiary anilines. The methylene carbon on N,N-dialkylanilines functioned as a source of one-carbon synthon in the reaction. The reaction used readily available starting materials, tolerated various functional groups, and afforded 2,4-disubstituted and 2,4,6-trisubstituted pyridines in good to high yields under mild conditions.