1224151-64-7

Basic information

• Product Name: (1R,2R)-1-amino-2-(2-isopropyl-4-methoxy-5-tert-butylbenzenamine)-1,2-di-tertbutylethane
• Synonyms: (1R,2R)-1-amino-2-(2-isopropyl-4-methoxy-5-tert-butylbenzenamine)-1,2-di-tertbutylethane
• CAS NO: 1224151-64-7
• Molecular Weight: 376.626
• Mol File: 1224151-64-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R,2R)-1-amino-2-(2-isopropyl-4-methoxy-5-tert-butylbenzenamine)-1,2-di-tertbutylethane(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-1-amino-2-(2-isopropyl-4-methoxy-5-tert-butylbenzenamine)-1,2-di-tertbutylethane(1224151-64-7)
• EPA Substance Registry System: (1R,2R)-1-amino-2-(2-isopropyl-4-methoxy-5-tert-butylbenzenamine)-1,2-di-tertbutylethane(1224151-64-7)

Safety Data

• Hazardous Substances Data: 1224151-64-7(Hazardous Substances Data)

Upstream product

• 879395-42-3 1-bromo-5-tert-butyl-2-isopropyl-4-methoxybenzene 
• 171357-23-6 (3R,4R)-3,4-diamino-2,2,5,5-tetramethylhexane 

Downstream Products

• 1224151-47-6 (4R,5R)-4,5-di-tert-butyl-1-(2-isopropyl-4-methoxy-5-tert-butylphenyl) imidazolidine 

Relevant articles and documents

Mechanistically inspired catalysts for enantioselective desymmetrizations by olefin metathesis

In asymmetric olefin metathesis reactions, the addition of halide additives is often required to augment enantioselectivities, despite the fact that the additives result in catalysts with diminished reactivities. The preparation of new chiral Ru-based catalysts was accomplished by exploiting previously reported mechanistic studies. The catalysts possess a high level of reactivity and successfully induce high levels of asymmetry in desymmetrization reactions without the use of halide additives.