112533-12-7

Basic information

• Product Name: 2-Buten-1-one, 4-hydroxy-1-(4-methoxyphenyl)-, (E)-
• CAS NO: 112533-12-7
• Molecular Formula: C11H12O3
• Molecular Weight: 192.214
• Mol File: 112533-12-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Buten-1-one, 4-hydroxy-1-(4-methoxyphenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Buten-1-one, 4-hydroxy-1-(4-methoxyphenyl)-, (E)-(112533-12-7)
• EPA Substance Registry System: 2-Buten-1-one, 4-hydroxy-1-(4-methoxyphenyl)-, (E)-(112533-12-7)

Safety Data

• Hazardous Substances Data: 112533-12-7(Hazardous Substances Data)

Upstream product

• 66107-29-7 4-methoxyphenyl triflate 
• 82994-41-0 (E)-3-(tri-n-butylstannyl)-2-propen-1-ol 
• 23147-58-2 glycolaldehyde dimer 
• 1777-55-5 (4-methoxyphenacylidene)triphenyl phosphorane 
• 123-11-5 4-methoxy-benzaldehyde 
• 24165-60-4 1-(4-methoxyphenyl)but-3-en-1-ol 
• 85234-21-5 1-(4-methoxyphenyl)but-3-en-1-one 

Downstream Products

• 1350725-21-1 2-(2-(4-methoxyphenyl)-2-oxoethyl)spiro[cyclopropane-1,2'-indene]-1',3'-dione 
• 1350725-13-1 (E)-4-(4-methoxyphenyl)-4-oxobut-2-en-1-yl diphenylphosphinate 
• 1362860-62-5 2-((2R,4S)-2-cyclohexyl-1,3-dioxolan-4-yl)-1-(4-methoxyphenyl)ethanone 
• 1362860-50-1 2-((2S,4S)-2-cyclohexyl-1,3-dioxolan-4-yl)-1-(4-methoxyphenyl)ethanone 
• 1447965-21-0 2-(2-cyclohexyl-3-tosyloxazolidin-4-yl)-1-phenylethanone 
• 1447965-22-1 2-(2-cyclohexyl-3-tosyloxazolidin-4-yl)-1-phenylethanone 
• 1447965-23-2 2-(2-(naphthalene-1-yl)-3-tosyloxazolodin-4-yl)-1-(4-(methoxy)phenyl)ethanone 
• 1447965-24-3 2-(2-(naphthalene-1-yl)-3-tosyloxazolodin-4-yl)-1-(4-(methoxy)phenyl)ethanone 
• 1449434-93-8 (R)-4-(2-(4-methoxyphenyl)-2-oxoethyl)-3-tosyloxazolidin-2-one 
• 1449435-02-2 (S)-4-(2-(4-methoxyphenyl)-2-oxoethyl)-3-tosyloxazolidin-2-one 

Relevant articles and documents

Lewis Acid Catalyzed [3+3] Annulation of Donor–Acceptor Cyclopropanes with γ-Hydroxyenones: Access to Highly Functionalized Tetrahydropyrans

Donor–acceptor cyclopropanes were engaged in a [3+3]-annulation reaction with γ-hydroxyenones. Sc(OTf)3was found to be the best catalyst, and 2,4,4,5-tetrasubstituted tetrahydropyran products were obtained in good yields under mild reaction con