1139922-16-9

Basic information

• Product Name: (S)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone
• Synonyms: (S)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone
• CAS NO: 1139922-16-9
• Molecular Weight: 267.371
• Mol File: 1139922-16-9.mol

Chemical Properties

• CAS DataBase Reference: (S)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone(1139922-16-9)
• EPA Substance Registry System: (S)-2-(1,2,3,4-tetrahydroquinolin-2-yl)-1-(3,4-dimethoxyphenyl)ethanone(1139922-16-9)

Safety Data

• Hazardous Substances Data: 1139922-16-9(Hazardous Substances Data)

Upstream product

• 95742-49-7 2-(4-methoxyphenethyl)quinoline 
• 5395-56-2 (E)-2-(2-(4-methoxyphenyl)vinyl)quinoline 

Relevant articles and documents

Highly enantioselective iridium-Catalyzed hydrogenation of 2-Benzylquinolines and 2-Functionalized and 2,3-disubstituted quinolines

The enantioselective hydrogenation of 2-benzylquinolines and 2-functionalized and 2,3-disubstituted quinohnes was developed by using the [Ir(COD)Cl]2/bisphosphine/I2 system with up to 96% ee. Moreover, mechanistic studies revealed the hydrogenation mechanism of quinoline involves a 1,4-hydride addition, isomerization, and 1,2-hydride addition, and the catalytic active species may be a Ir(III) complex with chloride and iodide.