52179-09-6

Basic information

• Product Name: ethyl 2-(4-vinylphenoxy)isobutyrate
• Synonyms: ethyl 2-(4-vinylphenoxy)isobutyrate;2-(4-Ethenylphenoxy)-2-methylpropanoic acid ethyl ester;Einecs 257-707-4
• CAS NO: 52179-09-6
• Molecular Formula: C₁₄H₁₈O₃
• Molecular Weight: 234.29092
• EINECS: 257-707-4
• Mol File: 52179-09-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 327.3°Cat760mmHg
• Flash Point: 134.8°C
• Appearance: /
• Density: 1.039g/cm³
• Vapor Pressure: 0.000203mmHg at 25°C
• Refractive Index: 1.522
• CAS DataBase Reference: ethyl 2-(4-vinylphenoxy)isobutyrate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(4-vinylphenoxy)isobutyrate(52179-09-6)
• EPA Substance Registry System: ethyl 2-(4-vinylphenoxy)isobutyrate(52179-09-6)

Safety Data

• Hazardous Substances Data: 52179-09-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H18O3/c1-5-11-7-9-12(10-8-11)17-14(3,4)13(15)16-6-2/h5,7-10H,1,6H2,2-4H3

Upstream product

• 7400-08-0 p-Coumaric Acid 
• 600-00-0 ethyl 2-bromoisobutyrate 
• 2628-17-3 4-Vinylphenol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 52179-28-9 ethyl 2-[4-(2,2-dichlorocyclopropyl)phenoxy]-2-methylpropionate 

Relevant articles and documents

TMSCFX2(X = Cl, Br) as halofluorocarbene sources for the synthesis of halofluorocyclopropanes

TMSCFX2 (X = Cl, Br; TMS = trimethylsilyl) have been developed as halofluorocarbene (CFX, X = Cl, Br) precursors for [2+1] cyclopropanation with alkenes. Structurally diverse halofluorocyclopropanes were obtained in good to excellent yields. It was found

Halocyclopropyl substituted phenoxyalkanoic acids

Halocyclopropyl substituted phenoxyalkanoic acids and esters thereof, having hypocholesteremic activity are prepared via several alternative synthetic approaches, involving as the key reactions interaction of a substituted phenylalkene with a carbene source to introduce the halocyclopropyl moiety, and reaction of a substituted phenol with chloroform and a lower-alkanone in the presence of base, or with a lower-alkyl α-bromo-alkanoate, to form the phenoxyalkanoic acid moiety.