20498-71-9

Basic information

• Product Name: Benzeneethanol, 4-methoxy-a-(4-methoxyphenyl)-
• CAS NO: 20498-71-9
• Molecular Formula: C16H18O3
• Molecular Weight: 258.317
• Mol File: 20498-71-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzeneethanol, 4-methoxy-a-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanol, 4-methoxy-a-(4-methoxyphenyl)-(20498-71-9)
• EPA Substance Registry System: Benzeneethanol, 4-methoxy-a-(4-methoxyphenyl)-(20498-71-9)

Safety Data

• Hazardous Substances Data: 20498-71-9(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 105-13-5 4-Methoxybenzyl alcohol 
• 637-69-4 4-Methoxystyrene 
• 459-64-3 4-methoxybenzenediazonium tetrafluoroborate 
• 123-11-5 4-methoxy-benzaldehyde 
• 475250-52-3 2-[(4-methoxyphenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 100-07-2 4-methoxy-benzoyl chloride 
• 119-52-8 4,4'-dimethoxybenzoin 
• 138744-94-2 1,2-bis(4-methoxyphenyl)-2-oxoethyl acetate 
• 64-17-5 ethanol 

Downstream Products

• 4705-34-4 1,2-bis(4-methoxyphenyl)ethene 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-09-4 4-methoxybenzoic acid 
• 79754-48-6 4,5-bis-(p-methoxyphenyl)pentanoic acid 
• 79754-57-7 7-methoxy-4-p-methoxybenzyl-1,2,3,4-tetrahydro-1-naphthol 
• 79754-56-6 7-methoxy-4-p-methoxybenzyl-3,4-dihydronaphthalen-1(2H)-one 
• 79754-54-4 7-hydroxy-4-p-hydroxybenzyl-1,2,3,4-tetrahydro-1-naphthol 
• 79754-55-5 4,5-bis-p-methoxyphenylpenta-2,4-dienoic acid 
• 79754-58-8 7-hydroxy-4-p-hydroxybenzyl-3,4-dihydronaphthalen-1(2H)-one 
• 79813-33-5 (+/-)-sequirin D 
• 79813-32-4 (+/-)-di-O-methylsequirin D 
• 1026218-12-1 3-[1,2-Bis-(4-methoxy-phenyl)-ethylsulfanyl]-propionic acid 
• 4705-34-4 4,4'-dimethoxystilbene 
• 145191-93-1 1-[1,2-Bis-(4-methoxy-phenyl)-ethyl]-1H-imidazole 

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

Synthesis of early-transition-metal carbide and nitride nanoparticles through the urea route and their use as alkylation catalysts

The use of urea as either a carbon or a nitrogen source enabled the synthesis of various early-transition-metal nitride and carbide nanoparticles (TiN, NbN, Mo2N, 2N, NbCxN1-x, Mo2 C and WC). The abil

REDUCTIVE COUPLING OF BENZOIC ACID HALIDES AND ESTERS USING LOW-VALENT TITANIUM

The reductive coupling of (substituted) benzoic acid chlorides and esters is achieved using low-valent titanium, generated from TiCl3 and LiAlH4.Both acid chlorides and esters seem to follow the same two reaction pathways: one path via tolanes to stilbenes, the other via benzils to complex mixtures of products arising from reduction and further coupling reactions.Although the exact product balance depends upon the reaction conditions the major product is (substituted) cis-stilbene.