4973-27-7

Basic information

• Product Name: 4-benzyl-2,6-di-tert-butylphenol
• Synonyms: Phenol, 2,6-bis(1,1-dimethylethyl)-4-(phenylmethyl)-
• CAS NO: 4973-27-7
• Molecular Formula: C₂₁H₂₈O
• Molecular Weight: 296.4464
• Mol File: 4973-27-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 364.3°C at 760 mmHg
• Flash Point: 167.1°C
• Density: 0.986g/cm³
• Vapor Pressure: 8.12E-06mmHg at 25°C
• Refractive Index: 1.539
• CAS DataBase Reference: 4-benzyl-2,6-di-tert-butylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-benzyl-2,6-di-tert-butylphenol(4973-27-7)
• EPA Substance Registry System: 4-benzyl-2,6-di-tert-butylphenol(4973-27-7)

Safety Data

• Hazardous Substances Data: 4973-27-7(Hazardous Substances Data)

Upstream product

• 128-39-2 2,6-di-tert-butylphenol 
• 104-54-1 3-Phenylpropenol 
• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 
• 100-63-0 phenylhydrazine 
• 7078-98-0 2,6-di-tert-butyl-4-benzylidene-cyclohexa-2,5-dienone 
• 121-44-8 triethylamine 
• 50-00-0 formaldehyd 
• 71-43-2 benzene 
• 719-22-2 2,6-Di-tert-butyl-1,4-benzoquinone 
• 6921-34-2 benzylmagnesium chloride 
• 101-53-1 p-benzylphenol 
• 115-11-7 isobutene 
• 96271-84-0 4-(α-benzoyloxy-benzylidene)-2,6-di-tert-butyl-cyclohexa-2,5-dienone 

Downstream Products

• 67341-92-8 2,6-di-tert-butyl-4-(methoxy(phenyl)methyl)phenol 
• 74233-05-9 4-Benzyl-2,6-di-tert-butyl-4-hydroperoxy-cyclohexa-2,5-dienone 
• 7078-98-0 2,6-di-tert-butyl-4-benzylidene-cyclohexa-2,5-dienone 

Relevant articles and documents

Uranyl-catalyzed hydrosilylation ofpara-quinone methides: access to diarylmethane derivatives

An efficient and convenient uranyl-catalyzed reductive hydrosilylation reaction ofpara-quinone methides (p-QMs) was developed by employing silane as the reductant. The hydrosilylation procedure using the UO2(NO3)2·6H2

B(C6F5)3-Catalyzed redox-neutral β-alkylation of tertiary amines using p -quinone methides via borrowing hydrogen

Herein, we present the first example of catalytic redox-neutral β-functionalization of tertiary amines through a borrowing hydrogen process. This B(C6F5)3-catalyzed procedure utilizes commercially or readily available cata

Antioxidant, preparation method therefor and application of antioxidant

The invention discloses an antioxidant. The antioxidant has a structure represented by a formula (I) shown in the description. The invention further discloses a preparation method for the antioxidant. The method comprises the following steps: (1) subjecti