110212-62-9

Basic information

• Product Name: 2-Butenedioic acid, 2,3-diphenyl-, diethyl ester, (E)-
• CAS NO: 110212-62-9
• Molecular Formula: C20H20O4
• Molecular Weight: 324.376
• Mol File: 110212-62-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-Butenedioic acid, 2,3-diphenyl-, diethyl ester, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butenedioic acid, 2,3-diphenyl-, diethyl ester, (E)-(110212-62-9)
• EPA Substance Registry System: 2-Butenedioic acid, 2,3-diphenyl-, diethyl ester, (E)-(110212-62-9)

Safety Data

• Hazardous Substances Data: 110212-62-9(Hazardous Substances Data)

Upstream product

• 5635-39-2 (Z)-2,3-diphenylbut-2-enedioic acid diethyl ester 
• 22065-57-2 ethyl 2-phenyldiazoacetate 
• 101-97-3 Ethyl 2-phenylethanoate 
• 769-92-6 4-tert-Butylaniline 
• 104-94-9 4-methoxy-aniline 
• 455-14-1 4-trifluoromethylphenylamine 
• 106-40-1 4-bromo-aniline 
• 106-47-8 4-chloro-aniline 
• 371-40-4 4-fluoroaniline 
• 62-53-3 aniline 
• 2882-19-1 ethyl 2-phenyl-2-bromoacetate 
• 7519-74-6 thiocamphor 
• 59176-55-5 ethyl α,α-dibromobenzeneacetate 
• 78-94-4 methyl vinyl ketone 

Downstream Products

• 79379-74-1 ethyl 1-oxo-2-phenyl-1H-indene-3-carboxylate 

Relevant articles and documents

Cinchona alkaloids induce asymmetry in the insertion reaction of thermally generated carbenes into N-H bonds

Ammonium ylides generated in situ from phenyldiazoacetates and anilines undergo asymmetric N-H insertion reactions catalyzed by cinchona alkaloids (1 mol %), affording phenylglycines up to 74% ee.

Catalytic O-H bond insertion reactions using surface modified sewage sludge as a catalyst

Developing a greener, sustainable catalyst is a very important but challenging task in organic synthesis. Herein, for the first time, we choose more economical and greener surface modified sewage sludge-derived carbonaceous materials (SW) treated by perch

S-Alkylation of Camphorthione with Diazo Esters

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