160560-18-9

Basic information

• Product Name: 1-(furan-3'-yl)-2-phenylethan-1-one
• Synonyms: 1-(furan-3'-yl)-2-phenylethan-1-one
• CAS NO: 160560-18-9
• Molecular Weight: 186.21
• Mol File: 160560-18-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-(furan-3'-yl)-2-phenylethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(furan-3'-yl)-2-phenylethan-1-one(160560-18-9)
• EPA Substance Registry System: 1-(furan-3'-yl)-2-phenylethan-1-one(160560-18-9)

Safety Data

• Hazardous Substances Data: 160560-18-9(Hazardous Substances Data)

Upstream product

• 488-93-7 3-Furoic acid 
• 103-82-2 phenylacetic acid 
• 148900-66-7 N-methoxy-N-methylfuran-3-carboxamide 
• 6921-34-2 benzylmagnesium chloride 
• 1185254-45-8 3-(1-methoxy-2-phenylvinyl)furan 
• 100-39-0 benzyl bromide 
• 201230-82-2 carbon monoxide 
• 87453-06-3 tributyl(furan-3-yl)stannane 
• 26420-79-1 1-chloro-3-benzyloxypropane 
• 90812-71-8 lithium furan-3-carboxylate 

Downstream Products

• 1283117-59-8 4-(3-ethoxy-4-hydroxy-5-nitrophenyl)-6-(furan-3-yl)-5-phenyl-3,4-dihydropyrimidin-2(1H)-one 

Relevant articles and documents

Total synthesis of (±)-kellermanoldione: stepwise cycloaddition of a functionalized diene and allenoate

Figur Presented The total synthesis of the diterpene kellermanoldione 1 is reported. Stepwise [4 + 2] cycloaddition of the ketal diene 8 and the allenoste 3 afforded the exo adduct 10x as the major product. It was converted into 1 via six steps, among them a key nonconjugative hydrolysis of a γ-methylene silyl enol ether

NOVEL DIHYDROPYRIMIDIN-2(1H)-ONE COMPOUNDS AS S-NITROSOGLUTATHIONE REDUCTASE INHIBITORS

The present invention is directed to novel dihydropyrimidin-2(1H)-one compounds useful as S-nitrosoglutathione reductase (GSNOR) inhibitors, pharmaceutical compositions comprising such compounds, and methods of making and using the same.

Regiospecific synthesis of 3,4-disubstituted furans and 3-substituted furans using 3,4-bis(tri-n-butylstannyl)furan and 3-(tri-n-butylstannyl)furan as building blocks

3,4-Bis(tri-n-butylstannyl)furan and 3-(tri-n-butylstannyl)furan have been prepared and used successfully as building blocks to lead to various 3,4-disubstituted furans and 3-substituted furans, respectively.