1372162-02-1

Basic information

• Product Name: ethyl 2-(3-(4-bromophenyl)-6,6-dimethyl-4-oxo-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate
• Synonyms: ethyl 2-(3-(4-bromophenyl)-6,6-dimethyl-4-oxo-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate
• CAS NO: 1372162-02-1
• Molecular Weight: 405.288
• Mol File: 1372162-02-1.mol

Chemical Properties

• CAS DataBase Reference: ethyl 2-(3-(4-bromophenyl)-6,6-dimethyl-4-oxo-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(3-(4-bromophenyl)-6,6-dimethyl-4-oxo-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate(1372162-02-1)
• EPA Substance Registry System: ethyl 2-(3-(4-bromophenyl)-6,6-dimethyl-4-oxo-4,5,6,7-tetrahydrobenzofuran-2-yl)acetate(1372162-02-1)

Safety Data

• Hazardous Substances Data: 1372162-02-1(Hazardous Substances Data)

Upstream product

• 117937-01-6 4-(4-bromophenyl)-4-hydroxybut-2-ynoic acid ethyl ester 
• 126-81-8 dimedone 
• 1394173-90-0 C₁₄H₁₄BrNO₆ 

Relevant articles and documents

A calcium catalysed regioselective (5-exo dig) tandem process for the synthesis of fully substituted furans

An efficient and highly regio-selective synthesis of fused & substituted furans has been described using Ca(OTf)2 as the catalyst. This tandem process involves alkylation, 5-exo dig cyclisation and isomerization to furnish densely substituted f

Efficient synthesis of tetrasubstituted furans from nitroallylic acetates and 1,3-dicarbonyl/α-activating ketones by Feist-Benary addition-elimination

Pure organic: The synthesis of tetrasubstituted furans often involves transition-metal catalysis or metal-halogen exchange reactions. A new approach to these heterocycles employs the Feist-Benary addition-elimination process using nitroallylic acetates an