122269-03-8

Basic information

• Product Name: Phenol, 2-(1,1-dimethylethyl)-4-(1,1-dimethylpropyl)-
• CAS NO: 122269-03-8
• Molecular Formula: C15H24O
• Molecular Weight: 220.355
• Mol File: 122269-03-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phenol, 2-(1,1-dimethylethyl)-4-(1,1-dimethylpropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-(1,1-dimethylethyl)-4-(1,1-dimethylpropyl)-(122269-03-8)
• EPA Substance Registry System: Phenol, 2-(1,1-dimethylethyl)-4-(1,1-dimethylpropyl)-(122269-03-8)

Safety Data

• Hazardous Substances Data: 122269-03-8(Hazardous Substances Data)

Upstream product

• 513-35-9 2-methyl-but-2-ene 
• 115-11-7 isobutene 
• 108-95-2 phenol 
• 80-46-6 4-t-amylphenol 
• 75-65-0 tert-butyl alcohol 

Downstream Products

• 1609538-01-3 C₁₅H₂₂O₂ 
• 108-95-2 phenol 

Relevant articles and documents

Controlling the catalytic aerobic oxidation of phenols

The oxidation of phenols is the subject of extensive investigation, but there are few catalytic aerobic examples that are chemo- and regioselective. Here we describe conditions for the ortho-oxygenation or oxidative coupling of phenols under copper (Cu)-catalyzed aerobic conditions that give rise to ortho-quinones, biphenols or benzoxepines. We demonstrate that each product class can be accessed selectively by the appropriate choice of Cu(I) salt, amine ligand, desiccant and reaction temperature. In addition, we evaluate the effects of substituents on the phenol and demonstrate their influence on selectivity between ortho-oxygenation and oxidative coupling pathways. These results create an important precedent of catalyst control in the catalytic aerobic oxidation of phenols and set the stage for future development of catalytic systems and mechanistic investigations.

Sterically hindered, regenerable Schiff base complexes, solutions thereof and process using the same

There are disclosed saltmen-type metallo Schiff base complexes and oxygen-sorbing and -desorbing solutions of the same, pressure- and temperature-swing oxygen separation processes using the complexes and solutions, and methods of regenerating such complexes and solutions.