19838-89-2

Basic information

• Product Name: 2-(4-methoxyphenyl)-1,1-diphenylethan-1-ol
• Synonyms: 2-(4-methoxyphenyl)-1,1-diphenylethan-1-ol
• CAS NO: 19838-89-2
• Molecular Weight: 304.389
• Mol File: 19838-89-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-(4-methoxyphenyl)-1,1-diphenylethan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxyphenyl)-1,1-diphenylethan-1-ol(19838-89-2)
• EPA Substance Registry System: 2-(4-methoxyphenyl)-1,1-diphenylethan-1-ol(19838-89-2)

Safety Data

• Hazardous Substances Data: 19838-89-2(Hazardous Substances Data)

Upstream product

• 14062-18-1 ethyl p-methoxyphenylacetate 
• 119-61-9 benzophenone 
• 475250-52-3 2-[(4-methoxyphenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 824-94-2 p-methoxybenzyl chloride 
• 23786-14-3 4-methoxy-phenyl acetic acid methyl ester 
• 100-58-3 phenylmagnesium bromide 
• 104-01-8 4-Methoxyphenylacetic acid 
• 2196-99-8 2-chloro-1-(4-methoxyphenyl)ethanone 
• 104-93-8 p-methylanizole 
• 67-64-1 acetone 

Downstream Products

• 1394025-02-5 2-[1-(4-methoxyphenyl)-2,2-diphenylvinyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane 
• 1394025-14-9 C₄₇H₃₇NO₂ 
• 1394025-16-1 C₅₉H₄₅NO₂ 
• 18648-74-3 2,2-diphenyl-1-(4-methoxyphenyl)ethylene 
• 25354-48-7 1-bromo-1-(p-methoxyphenyl)-2,2-diphenylethene 

Relevant articles and documents

A Photoredox Coupling Reaction of Benzylboronic Esters and Carbonyl Compounds in Batch and Flow

Mild cross-coupling reaction between benzylboronic esters with carbonyl compounds and some imines was achieved under visible-light-induced iridium-catalyzed photoredox conditions. Functional group tolerance was demonstrated by 51 examples, including 13 he

Palladium-catalysed direct synthesis of benzo[b]thiophenes from thioenols

The one-pot conversion of thioenols into benzo[b]thiophenes was achieved by using a simple palladium catalyst such as PdCl2 or PdCl 2(cod). The Royal Society of Chemistry.