60336-03-0

Basic information

• Product Name: ethyl 5-(4-chlorophenyl)furan-2-carboxylate
• Synonyms: ethyl 5-(4-chlorophenyl)furan-2-carboxylate
• CAS NO: 60336-03-0
• Molecular Weight: 250.682
• Mol File: 60336-03-0.mol

Chemical Properties

• CAS DataBase Reference: ethyl 5-(4-chlorophenyl)furan-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 5-(4-chlorophenyl)furan-2-carboxylate(60336-03-0)
• EPA Substance Registry System: ethyl 5-(4-chlorophenyl)furan-2-carboxylate(60336-03-0)

Safety Data

• Hazardous Substances Data: 60336-03-0(Hazardous Substances Data)

Upstream product

• 6132-37-2 ethyl 5-bromofuran-2-carboxylate 
• 5575-51-9 tris(4-chlorophenyl)bismuthane 
• 41019-45-8 5-(4-chlorophenyl)-2-furoic acid 
• 64-17-5 ethanol 
• 106-39-8 bromochlorobenzene 

Downstream Products

• 1312579-17-1 C₂₀H₁₅BrClNO₆ 
• 1357089-50-9 C₃₂H₃₂ClN₃O₆ 
• 1357089-52-1 C₃₂H₃₂ClN₃O₅ 
• 1312579-06-8 C₃₀H₂₆ClN₃O₄ 
• 1312579-07-9 C₃₇H₃₁BrClN₃O₄ 
• 1312579-08-0 C₄₂H₃₅ClN₄O₄ 
• 1312578-79-2 C₃₄H₂₉ClN₄O₂ 
• 1312579-18-2 C₃₀H₃₁ClN₂O₈ 
• 1312578-77-0 C₂₉H₂₅BrClN₃O₂ 
• 1312578-76-9 C₂₈H₂₅ClN₄O₂ 
• 1312578-82-7 C₂₄H₂₂ClF₂N₃O₂ 
• 1312578-84-9 C₂₆H₂₆ClN₃O₂ 
• 1435946-84-1 C₂₅H₂₄ClN₃O₂ 

Relevant articles and documents

Triflic Acid-Catalyzed Cycloisomerization Reactions of Donor-Acceptor Cyclopropanes: Access to Alkyl 5-Arylfuran-2-carboxylates

A direct synthetic strategy starting from alkyl 1-alkoxy-2-aroylcyclopropanecarboxylates was developed for the construction of alkyl 5-arylfuran-2-carboxylates. These donor-acceptor cyclopropanes smoothly undergo a simple ring-opening reaction or/and cycl

Mono- and biscouplings using triarylbismuths for the atom-efficient arylations of functionalized furans under palladium catalysis

Palladium-catalyzed cross-coupling reactions of functionalized bromofurans with triarylbismuths have been described for the atom-economic synthesis of functionalized arylfuran systems. The coupling reactions using triarylbismuths with various 2-bromofurans and 2,5-dibromofuran underwent smoothly to afford the corresponding 2-arylfurans and 2,5-diarylfurans in high yields in a short reaction time (one hour). Georg Thieme Verlag Stuttgart · New York.

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