31603-95-9

Basic information

• Product Name: tert-butyl 4-tert-butylphenyl ether
• Synonyms: 1-tert-Butoxy-4-tert-butylbenzene; benzene, 1-(1,1-dimethylethoxy)-4-(1,1-dimethylethyl)-; tert-Butyl 4-tert-butylphenyl ether
• CAS NO: 31603-95-9
• Molecular Formula: C₁₄H₂₂O
• Molecular Weight: 206.3239
• Mol File: 31603-95-9.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 267.1°C at 760 mmHg
• Flash Point: 119.2°C
• Density: 0.898g/cm³
• Vapor Pressure: 0.0137mmHg at 25°C
• Refractive Index: 1.479
• CAS DataBase Reference: tert-butyl 4-tert-butylphenyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 4-tert-butylphenyl ether(31603-95-9)
• EPA Substance Registry System: tert-butyl 4-tert-butylphenyl ether(31603-95-9)

Safety Data

• Hazardous Substances Data: 31603-95-9(Hazardous Substances Data)

Upstream product

• 98-54-4 para-tert-butylphenol 
• 115-11-7 isobutene 
• 75-65-0 tert-butyl alcohol 
• 108-95-2 phenol 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 865-48-5 sodium t-butanolate 
• 98946-18-0 tert-Butyl 2,2,2-trichloroacetimidate 
• 75-97-8 3,3-dimethyl-butan-2-one 
• 507-20-0 tertiary butyl chloride 

Downstream Products

• 93332-08-2 3,5-dinitro-benzoic acid-(4-tert-butyl-phenyl ester) 
• 16222-41-6 tert-butyl 4-fluorophenyl ether 
• 507262-32-0 4-tert-butyl-4-fluorocyclohexa-2,5-dien-1-one 
• 98-54-4 para-tert-butylphenol 
• 223768-46-5 4-tert-butyl-2-bromo-1-tert-butyloxy-benzene 

Relevant articles and documents

Catalytic organic solid gas reaction: Kinetic and mechanism

The alkylation of solid 4-tertiobutylphenol by gaseous isobutene in the presence of a catalyst has been studied according to different parameters such as, temperature, initial pressure of isobutene, proportion of catalyst and the granulometry of the catalyst and the solid reactant. Among the predefined kinetic models, the unreacted core model for spherical particles of unchanging size is the best adapted to the experimental results. Based on this model, a mechanism is proposed involving the intervention of a carbocation.

Palladium-catalyzed formation of aryl tert-butyl ethers from unactivated aryl halides

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Palladium-catalyzed C-O coupling involving unactivated aryl halides. Sterically induced reductive elimination to form the C-O bond in diaryl ethers [4]

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