129626-52-4

Basic information

• Product Name: 3-[5-(2-BROMO-PHENYL)-FURAN-2-YL]-ACRYLIC ACID
• Synonyms: 3-[5-(2-BROMO-PHENYL)-FURAN-2-YL]-ACRYLIC ACID
• CAS NO: 129626-52-4
• Molecular Formula: C₁₃H₉BrO₃
• Molecular Weight: 293.11
• Mol File: 129626-52-4.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-[5-(2-BROMO-PHENYL)-FURAN-2-YL]-ACRYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[5-(2-BROMO-PHENYL)-FURAN-2-YL]-ACRYLIC ACID(129626-52-4)
• EPA Substance Registry System: 3-[5-(2-BROMO-PHENYL)-FURAN-2-YL]-ACRYLIC ACID(129626-52-4)

Safety Data

• Hazardous Substances Data: 129626-52-4(Hazardous Substances Data)

Upstream product

• 141-82-2 malonic acid 
• 58110-57-9 5-(2-bromophenyl)furan-2-carboxaldehyde 

Downstream Products

• 129626-58-0 2-(2-Bromo-phenyl)-5-[(E)-2-(2-bromo-phenyl)-vinyl]-furan 

Relevant articles and documents

ARYLATION OF FURAN COMPOUNDS BY ARENEDIAZONIUM SALTS

3-(5-Aryl-2-furyl)acrylic acids were obtained by the reaction of 5-arylfurfurals with malonic acid.They were arylated by diazonium salts with decarboxylation and the formation of 5-aryl-2-styrylfurans.The latter were also obtained by the interaction of furylacrolein with diazonium salts.This reaction also gave 3-(5-aryl-2-furyl)acroleins and the corresponding arylfurylacrylic acids, which were arylated again with the release of CO2 and the formation of 5-aryl-2-styrylfurans. 3-(5-Aryl-2-furyl)acroleins were also synthesized by the condensation of 5-arylfurfurals with acetaldehyde under phase-transfer conditions.The s-trans configuration of the furan ring and the exocyclic double bond were established in the obtained compounds by the PMR method.