24973-57-7

Basic information

• Product Name: 2-amino-3,5-ditert-butylphenol
• Synonyms: 2-amino-3,5-ditert-butylphenol
• CAS NO: 24973-57-7
• Molecular Formula: C₁₄H₂₃NO
• Molecular Weight: 221.33852
• Mol File: 24973-57-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-amino-3,5-ditert-butylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-3,5-ditert-butylphenol(24973-57-7)
• EPA Substance Registry System: 2-amino-3,5-ditert-butylphenol(24973-57-7)

Safety Data

• Hazardous Substances Data: 24973-57-7(Hazardous Substances Data)

Upstream product

• 1138-52-9 3,5-Di-tert-butylphenol 
• 3114-67-8 2-Nitro-3,5-di-tert-butyl-phenol 

Downstream Products

• 1338078-86-6 4-tBu-6-CMe₂Ph-2-CH=N(4,6-tBu₂-2-OHC₆H₂)C₆H₂OH 
• 328105-09-5 2,4-di-tert-butyl-6-{[(2-hydroxy-3,5-di-tert-butylphenyl)methylene]amino}phenol 
• 1338078-85-5 4-tBu-6-Ad-2-CH=N(4,6-tBu₂-2-OHC₆H₂)C₆H₂OH 
• 91054-21-6 2,4-di-tert-butyl-6-iminocyclohexa-2,4-dienoneine 
• 3383-21-9 3,5-di-tert-butyl-o-benzoquinone 
• 24973-56-6 2-benzoylamino-3,5-di-tert-butyl-phenol 
• 25068-98-8 N-(2,4-Di-tert-butyl-6-methoxy-phenyl)-benzamide 
• 25068-99-9 4,6-di-tert-butyl-2-phenyl-benzooxazole 

Relevant articles and documents

Electrochemical and Spectroscopic Studies of 3,5-Di-tert-butyl-2-aminophenol and of Electrosynthesized 3,5-Di-tert-butyl-2-iminocyclohexa-3,5-dienone in Aprotic Solvents

In acetonitrile 3,5-di-tert-butyl-2-iminocyclohexa-3,5-dienone (DTBQI) is the major product from the controlled-potential electrooxidation of 3,5-di-tert-butyl-2-aminophenol (DTBAPH2).The same product results from the chemical oxidation of DTBAPH2 by PbO2.The redox chemistry for DTBAPH2, DTBQI, and o-aminophenol in dimethyl sulfoxide and acetonitrile has been studied with cyclic voltammetry and controlled-potential electrolysis, and the products and intermediates have been characterized by 1H and 13C NMR, ESR, IR, and UV-vis spectroscopy.Addition of strong base (OH-) to DTBQI causes it to be reduced to a product with the characteris tics of DTBAPH-.Redox reaction mechanisms are proposed for the electrochemical oxidation of DTBAPH- to DTBQI and for the latter's reduction.