134822-96-1

Basic information

• Product Name: 1-(tert-butyl)-4-(4-methoxyphenoxy)benzene
• Synonyms: 1-(tert-butyl)-4-(4-methoxyphenoxy)benzene
• CAS NO: 134822-96-1
• Molecular Weight: 256.345
• Mol File: 134822-96-1.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-(tert-butyl)-4-(4-methoxyphenoxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(tert-butyl)-4-(4-methoxyphenoxy)benzene(134822-96-1)
• EPA Substance Registry System: 1-(tert-butyl)-4-(4-methoxyphenoxy)benzene(134822-96-1)

Safety Data

• Hazardous Substances Data: 134822-96-1(Hazardous Substances Data)

Upstream product

• 98-54-4 para-tert-butylphenol 
• 5720-07-0 4-methoxyphenylboronic acid 
• 696-62-8 para-iodoanisole 
• 3972-56-3 4-(tert-butyl)chlorobenzene 
• 150-76-5 4-methoxy-phenol 
• 100-17-4 para-methoxynitrobenzene 
• 142342-33-4 4,4'-di(tert-butyl)diphenyliodonium tosylate 
• 253185-03-4 tert-butylbenzene 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 12775-96-1 copper 
• 1122-95-8 sodium 4-methoxyphenolate 

Downstream Products

• 150-76-5 4-methoxy-phenol 

Relevant articles and documents

Pd-Catalyzed Etherification of Nitroarenes

The Pd-catalyzed etherification of nitroarenes with arenols has been achieved using a new rationally designed ligand. Mechanistic insights were used to design the ligand so that both the oxidative addition and reductive elimination steps of a plausible catalytic cycle were facilitated. The catalytic system established here provides direct access to a range of unsymmetrical diaryl ethers from nitroarenes.

Aromatic ether compound or the sulfhydryl compound

[Problem] Aromatic ether compounds and aromatic sulfide compound of this new technology to[Solution] In general formula (1a), (1b), (1c) palladium or nickel compound or a phosphine compound represented by the compound comprising a transition metal compound in the presence of a transition metal catalyst, (A1) is represented by compounds having hydroxy carbon C a-OH or (A2) with a compound represented by the sulfhydryl carbon C a-SH, nitro group (- NO2 ) To react with an aromatic nitro compound (B), (A1) to the compound of the aromatic nitro compound (C1) or the reaction product of an aromatic ether compounds (B) hetero coupling (A2) of the compounds of the reaction product of an aromatic sulfide compound of an aromatic nitro compound (C2) generating (B) hetero coupling characterized by comprising the step of, aromatic ether compounds or aromatic sulfide compound. [Drawing] no

The coupling reactions of aryl halides and phenols catalyzed by palladium and MOP-type ligands

Palladium-catalyzed coupling reactions of aryl halides and phenols are described employing the bulky and electron-rich MOP-type ligands. When K3PO4 was used as base and toluene as solvent, the catalyst system exhibited high efficiency for the coupling reaction of the activated aryl halides. When NaH was used as base and o-xylene as solvent, unactivated aryl halides can be used as substrates.