152-78-3

Basic information

• Product Name: 3,4-bis-(4-methoxyphenyl)-1,2-dihydronaphthalene
• Synonyms: 3,4-bis-(4-methoxyphenyl)-1,2-dihydronaphthalene
• CAS NO: 152-78-3
• Molecular Weight: 342.437
• Mol File: 152-78-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,4-bis-(4-methoxyphenyl)-1,2-dihydronaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-bis-(4-methoxyphenyl)-1,2-dihydronaphthalene(152-78-3)
• EPA Substance Registry System: 3,4-bis-(4-methoxyphenyl)-1,2-dihydronaphthalene(152-78-3)

Safety Data

• Hazardous Substances Data: 152-78-3(Hazardous Substances Data)

Upstream product

• 93296-09-4 4-methoxyphenylzinc chloride 
• 696-62-8 para-iodoanisole 
• 141339-54-0 bis(4-anisyl)iodonium triflate 

Downstream Products

• 1383673-34-4 1,2-bis(4-methoxyphenyl)naphthalene 

Relevant articles and documents

An Interrupted Pummerer/Nickel-Catalysed Cross-Coupling Sequence

An interrupted Pummerer/nickel-catalysed cross-coupling strategy has been developed and used in the elaboration of styrenes. The operationally simple method can be carried out as a one-pot process, involves the direct formation of stable alkenyl sulfonium salt intermediates, utilises a commercially available sulfoxide, catalyst, and ligand, operates at ambient temperature, accommodates sp-, sp2-, and sp3-hybridised organozinc coupling partners, and delivers functionalised styrene products in high yields over two steps. An interrupted Pummerer/cyclisation approach has also been used to access carbo- and heterocyclic alkenyl sulfonium salts for cross-coupling.

ADRENAL CORTICAL INHIBITORS AND POTENT SYNTHETIC ESTROGENS.

-