1256350-54-5

Basic information

• Product Name: 3-(3,5-dimethoxyphenyl)-6-methoxy-2-(4-methoxyphenyl)benzofuran-4-carboxylic acid
• Synonyms: 3-(3,5-dimethoxyphenyl)-6-methoxy-2-(4-methoxyphenyl)benzofuran-4-carboxylic acid
• CAS NO: 1256350-54-5
• Molecular Weight: 434.445
• Mol File: 1256350-54-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3-(3,5-dimethoxyphenyl)-6-methoxy-2-(4-methoxyphenyl)benzofuran-4-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3,5-dimethoxyphenyl)-6-methoxy-2-(4-methoxyphenyl)benzofuran-4-carboxylic acid(1256350-54-5)
• EPA Substance Registry System: 3-(3,5-dimethoxyphenyl)-6-methoxy-2-(4-methoxyphenyl)benzofuran-4-carboxylic acid(1256350-54-5)

Safety Data

• Hazardous Substances Data: 1256350-54-5(Hazardous Substances Data)

Upstream product

• 118112-18-8 3,5-dimethoxybicyclo[4.2.0]octa-1⁽⁶⁾,2,4-trien-7-one 
• 1422375-82-3 2-iodo-3,5-dimethoxybenzonitrile 
• 19179-31-8 3,5-dimethoxy-benzonitrile 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 74726-77-5 2-iodo-3,5-bis(methoxy)benzenemethanol 
• 153786-93-7 2-iodo-3,5-dimethoxybenzyl acetate 
• 1180491-74-0 methyl 3-(3,5-dimethoxyphenyl)-6-methoxy-2-(4-methoxyphenyl)-benzofuran-4-carboxylate 

Downstream Products

• 1190948-58-3 4,7,9-trihydroxy-1-(4-hydroxyphenyl)-6H-anthra[1,9-bc]furan-6-one 
• 1256350-46-5 4,7,9-trimethoxy-1-(4-methoxyphenyl)-6H-anthra[1,9-bc]furan-6-one 

Relevant articles and documents

Reinvestigating the acyl cyclization to the precursor of diptoindonesin G

We reinvestigated the synthesis of the precursor of diptoindonesin G (2) by the intramolecular acyl cyclization of compound 1 or compound 3 in the presence of trifluoroacetic anhydride (TFAA) [1,2]. Although the reaction of 3 with TFAA generated 2 smoothl

SYNTHESIS OF NOVEL ANALOGS OF DIPTOINDONESIN G, COMPOUNDS FORMED THEREBY, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

Disclosed are unnatural analogs of Diptoindonesin G, methods to make the analogs, pharmaceutical compositions containing the analogs, and methods of using the analogs to inhibit neoplastic cell growth.

Symmetry-based approach to oligostilbenoids: Rapid entry to viniferifuran, shoreaphenol, malibatol A, and diptoindonesin G

The recognition of the local symmetric image within benzofuran-based natural oligostilbenoids guided us to design a modular synthetic approach to these molecules by utilizing a three-step sequence consisting of Sonogashira coupling, iodocyclization, and S