24457-06-5

Basic information

• Product Name: 2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-hydroxy-4-phenyl-
• CAS NO: 24457-06-5
• Molecular Formula: C20H26O2
• Molecular Weight: 298.425
• Mol File: 24457-06-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-hydroxy-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-hydroxy-4-phenyl-(24457-06-5)
• EPA Substance Registry System: 2,5-Cyclohexadien-1-one, 2,6-bis(1,1-dimethylethyl)-4-hydroxy-4-phenyl-(24457-06-5)

Safety Data

• Hazardous Substances Data: 24457-06-5(Hazardous Substances Data)

Upstream product

• 2668-47-5 2,6-di(t-butyl)-4-phenylphenol 
• 2525-38-4 2,6-di-tert-butyl-4-phenylphenoxyl 

Downstream Products

• 24456-99-3 5-phenyl-3-t-butyl-1,2-benzoquinone 
• 68757-75-5 5-methoxy-3-t-butyl-1,1'-biphenyl-4-ol 
• 2668-47-5 2,6-di(t-butyl)-4-phenylphenol 
• 68757-74-4 4-methoxy-4-phenyl-2,6-di-t-butylcyclohexa-2,5-dienone 
• 83638-55-5 5-acetylthio-3-t-butyl-1,1'-biphenyl-4-yl acetate 
• 83638-64-6 4-acetylthio-4-phenyl-2,6-di-t-butylcyclohexa-2,5-dienone 
• 83638-56-6 2-methyl-6-phenyl-4-t-butylbenzo-1,3-dioxole 
• 83638-66-8 4-(2-methylprop-2-enyl)-4-phenyl-2,6-di-t-butylcyclohexa-2,5-dienone 
• 68757-66-4 4-hydroxy-5-t-butyl-1,1'-biphenyl-3-yl acetate 
• 68757-65-3 5-t-butyl-1,1'-biphenyl-3,4-diyl diacetate 
• 83638-54-4 3-hydroxy-5-t-butyl-1,1'-biphenyl-4-yl acetate 
• 83638-52-2 3-(3-acetoxy-5-t-butyl-1,1'-biphenyl-4-oxy)-5-t-butyl-1,1'-biphenyl-4-ol 
• 68757-64-2 4-acetoxy-4-phenyl-2,6-di-t-butylcyclohexa-2,5-dienone 
• 83638-65-7 3-(3'-acetoxy-5-t-butyl-1,1'-biphenyl-4-oxy)-5-t-butyl-1,1'-biphenyl-4-yl acetate 

Relevant articles and documents

Field control of regioselectivity in CoIII(salpr)(OH) promoted oxygenation of 4-aryl-2,6-di-terf-butylphenols

In the CoIII(salpr)(OH) catalyzed oxygenation of 4-aryl-2,6-di-tert-butylphenols, the position of dioxygen incorporation is completely controlled by the nature of solvent; dioxygen incorporation occurs only at ortho position in an uncoordinativ