107150-74-3

Basic information

• Product Name: Benzeneacetic acid, 3-(ethoxycarbonyl)-, ethyl ester
• CAS NO: 107150-74-3
• Molecular Formula: C13H16O4
• Molecular Weight: 236.268
• Mol File: 107150-74-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzeneacetic acid, 3-(ethoxycarbonyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, 3-(ethoxycarbonyl)-, ethyl ester(107150-74-3)
• EPA Substance Registry System: Benzeneacetic acid, 3-(ethoxycarbonyl)-, ethyl ester(107150-74-3)

Safety Data

• Hazardous Substances Data: 107150-74-3(Hazardous Substances Data)

Upstream product

• 24398-88-7 ethyl 3-bromobenzoate 
• 105-53-3 diethyl malonate 
• 54589-54-7 ethyl 3-(chloromethyl)benzoate 
• 541-41-3 chloroformic acid ethyl ester 
• 16532-78-8 3-(cyanomethyl)benzonitrile 
• 64-17-5 ethanol 
• 2084-13-1 3-carboxymethyl-benzoic acid 

Downstream Products

• 155938-40-2 3'-carboxymethylflavone methyl ester 
• 155938-67-3 3-carboethoxymethylbenzoyl chloride 
• 155938-46-8 [3-(4-Oxo-4H-chromen-2-yl)-phenyl]-acetic acid hexadecyl ester 
• 155938-45-7 [3-(4-Oxo-4H-chromen-2-yl)-phenyl]-acetic acid octyl ester 
• 155938-29-7 [3-(5,7-Dimethyl-4-oxo-4H-chromen-2-yl)-phenyl]-acetic acid ethyl ester 
• 155938-25-3 [3-(6-Methyl-4-oxo-4H-chromen-2-yl)-phenyl]-acetic acid ethyl ester 
• 155938-43-5 [3-(4-Oxo-4H-chromen-2-yl)-phenyl]-acetic acid butyl ester 
• 155938-44-6 [3-(4-Oxo-4H-chromen-2-yl)-phenyl]-acetic acid isobutyl ester 
• 155938-41-3 [3-(4-Oxo-4H-chromen-2-yl)-phenyl]-acetic acid propyl ester 
• 155938-42-4 [3-(4-Oxo-4H-chromen-2-yl)-phenyl]-acetic acid isopropyl ester 
• 155938-69-5 3'-carboxymethylflavone ethyl ester 

Relevant articles and documents

Copper-Catalyzed Ullmann-Type Coupling and Decarboxylation Cascade of Arylhalides with Malonates to Access α-Aryl Esters

We have developed a high-efficiency and practical Cu-catalyzed cross-coupling to directly construct versatile α-aryl-esters by utilizing readily available aryl bromides (or chlorides) and malonates. These gram-scale approaches occur with turnovers of up to 1560 and are smoothly conducted by the usage of a low catalyst loading, a new available ligand, and a green solvent. A variety of functional groups are tolerated, and the application occurs with α-aryl-esters to access nonsteroidal anti-inflammatory drugs (NSAIDs) on the gram scale.

Synthesis and hypolipidemic activity of novel 4-oxo- and 4-thioxo-4H-benzopyran-2-phenylalkanoic acids and esters

Novel 4-oxo- and 4-thioxo-4H-benzopyran-2-phenylalkanoic acids and esters have been prepared and evaluated for their hypolipidemic activity.Among these compounds 3'-alkanoyl derivatives show superior activity, decreasing total cholesterol, triglycerides a