5963-51-9

Basic information

• Product Name: Benzene, 1,1'-(1,2-ethanediyl)bis[3,4-diMethoxy-
• Synonyms: Benzene, 1,1'-(1,2-ethanediyl)bis[3,4-diMethoxy-;1,2-Bis(3,4-diMethoxyphenyl)ethane
• CAS NO: 5963-51-9
• Molecular Formula: C₁₈H₂₂O₄
• Molecular Weight: 302.36488
• Mol File: 5963-51-9.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzene, 1,1'-(1,2-ethanediyl)bis[3,4-diMethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-(1,2-ethanediyl)bis[3,4-diMethoxy-(5963-51-9)
• EPA Substance Registry System: Benzene, 1,1'-(1,2-ethanediyl)bis[3,4-diMethoxy-(5963-51-9)

Safety Data

• Hazardous Substances Data: 5963-51-9(Hazardous Substances Data)

Usage

General Description

Benzene, 1,1'-(1,2-ethanediyl)bis[3,4-dimethoxy- is a chemical compound with the molecular formula C20H24O4. It is a diether derivative of benzene and contains two methoxy groups attached to each of the benzene rings. Benzene, 1,1'-(1,2-ethanediyl)bis[3,4-dimethoxy- is often used as a building block in the synthesis of various organic compounds and pharmaceuticals. It may also have potential applications in the fields of materials science and drug development. However, it is important to handle and use this chemical with caution due to its potential health hazards and toxicity.

Upstream product

• 18513-98-9 3,4,3',4'-Tetramethoxystilben 
• 554-34-7 1,2-bis(3,4-dimethoxyphenyl)ethane-1,2-dione 
• 53751-40-9 veratryl acetate 
• 21852-32-4 4-bromomethyl-1,2-dimethoxybenzene 
• 17745-86-7 3,4-dimethoxybenzaldehyde N-[-(3,4-dimethoxyphenyl)methylidene] hydrazone 
• 79238-81-6 4-[(3,4-dimethoxyphenyl)ethynyl]-1,2-dimethoxybenzene 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 2859-78-1 4-Bromoveratrole 
• 54370-01-3 1-bromo-2-(chloromethyl)-4,5-dimethoxy-benzene 
• 5385-62-6 3,3’,4,4’-tetramethoxystilbene 
• 7417-21-2 2-(3,4-dimethoxyphenyl)ethyl alcohol 
• 859942-25-9 1,2-bis(2-bromo-4,5-dimethoxyphenyl)ethane 
• 7575-08-8 4-[(Z)-2-(3,4-dimethoxyphenyl)vinyl]-1,2-dimethoxybenzene 
• 157843-80-6 3,4-Dimethoxybenzyl pivalate 

Downstream Products

• 857565-65-2 1-(4,5,3',4'-tetramethoxy-bibenzyl-2-yl)-ethanone 
• 102752-21-6 bibenzyltetrayl-(3.4.3'.4')-tetraacetate 
• 55087-26-8 4,5,3',4'-tetramethoxy-bibenzyl-2-carboxylic acid 
• 859942-25-9 1,2-bis(2-bromo-4,5-dimethoxyphenyl)ethane 
• 859942-26-0 3,3’,4,4’-tetramethoxy-6,6’-diiodobibenzyl 
• 3842-68-0 4,4'-(ethane-1,2-diyl)dibenzene-1,2-diol 

Relevant articles and documents

A concise palladium-catalyzed carboamination route to (±)- tylophorine

(Chemical Equation Presented) Atotal synthesis of the racemic natural product tylophorine [(±)-1] has been demonstrated using the palladium-catalyzed carboamination method developed byWolfe and co-workers. In this case, an electron-rich aryl bromide 18 wa

Luminescent tungsten(vi) complexes as photocatalysts for light-driven C-C and C-B bond formation reactions

The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten(vi) complex which can be conveniently prepared at the gram-scale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C-C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance.

Dihedral-Angle-Controlled Crossover from Static Hole Delocalization to Dynamic Hopping in Biaryl Cation Radicals

In cases of coherent charge-transfer mechanism in biaryl compounds the rates follow a squared cosine trend with varying dihedral angle. Herein we demonstrate using a series of biaryl cation radicals with varying dihedral angles that the hole stabilization