185249-90-5

Basic information

• Product Name: 1-(3,4-dimethoxyphenyl)-2-(3',5'-dimethoxyphenyl)ethan-1-ol
• Synonyms: 1-(3,4-dimethoxyphenyl)-2-(3',5'-dimethoxyphenyl)ethan-1-ol
• CAS NO: 185249-90-5
• Molecular Weight: 318.37
• Mol File: 185249-90-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-(3,4-dimethoxyphenyl)-2-(3',5'-dimethoxyphenyl)ethan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4-dimethoxyphenyl)-2-(3',5'-dimethoxyphenyl)ethan-1-ol(185249-90-5)
• EPA Substance Registry System: 1-(3,4-dimethoxyphenyl)-2-(3',5'-dimethoxyphenyl)ethan-1-ol(185249-90-5)

Safety Data

• Hazardous Substances Data: 185249-90-5(Hazardous Substances Data)

Upstream product

• 110-71-4 1,2-dimethoxyethane 
• 14064-41-6 (E)-3-methoxystilbene 
• 120078-23-1 1-(3,4-dimethoxyphenyl)-2-(3,5-dimethoxyphenyl)ethanone 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 185249-83-6 3,5-dimethoxybenzyl trimethylsilyl ether 
• 6652-32-0 3,5-dimethoxybenzylchloride 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 56723-83-2 2-(3,5-dimethoxyphenyl)nitroethane 
• 86255-43-8 trans-1-(3,5-Dimethoxyphenyl)-2-nitroethylene 
• 15601-07-7 2-(3,5-dimethoxyphenyl)acetyl chloride 
• 1097-21-8 Azalactone of α-benzoylamino-β-(3,5-dimethoxyphenyl)acrylic acid 
• 4670-10-4 (3,5-dimethoxyphenyl)acetic acid 
• 7311-34-4 3,5-dimethoxybenzaldehdye 

Downstream Products

• 83088-26-0 (E)-tetramethylpiceatannol 
• 10083-24-6 trans-piceatannol 
• 22318-87-2 3,5,4',5'-tetramethoxydihydrostilbene 

Relevant articles and documents

Convenient syntheses of 3-aryl-3,4-dihydroisocoumarins

A convenient method for the synthesis of naturally occurring 3,4-dihydroisocoumarins by judicious use of Friedel-Craft acylation, regioselective formylation and oxidative cyclisation reactions is described. O-methylated analogues of montroumarin and thunb

Benzylic Manganese Halides, Sulfonates, and Phosphates: Preparation, Coupling Reactions, and Applications in Organic Synthesis

The use of highly active manganese, prepared by the Rieke method, for the direct preparation of benzylic manganese reagents was investigated. The oxidative addition of the highly active manganese (Mn*) to benzylic halides was easily completed under mild conditions. More importantly, benzylic manganese sulfonates and phosphates were prepared by direct oxidative addition of Mn* to the carbon-oxygen bonds of benzylic sulfonates and phosphates. The resulting benzylic manganese reagents were found to undergo cross-coupling reactions with a variety of electrophiles. The majority of these reactions were carried out in the absence of any transition metal catalyst under mild conditions. This approach also provided a facile synthetic route to the preparation of resorcinolic lipids.

Combretastatin Analogs via Hydration of Stilbene Derivatives

Hydration of the double bond of some stilbene congeners of Picea abies bark by TiCl4.NaBH4 reagent is described.Five racemic 1,2-diphenylethanol derivatives (9-13), structurally related to (R)-(-)combretastatin , have been obtained and characterize