10036-17-6

Basic information

• Product Name: Benzoic acid, 3-(3-ethoxy-3-oxo-1-propenyl)-, ethyl ester
• CAS NO: 10036-17-6
• Molecular Formula: C14H16O4
• Molecular Weight: 248.279
• Mol File: 10036-17-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-(3-ethoxy-3-oxo-1-propenyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-(3-ethoxy-3-oxo-1-propenyl)-, ethyl ester(10036-17-6)
• EPA Substance Registry System: Benzoic acid, 3-(3-ethoxy-3-oxo-1-propenyl)-, ethyl ester(10036-17-6)

Safety Data

• Hazardous Substances Data: 10036-17-6(Hazardous Substances Data)

Upstream product

• 93-89-0 benzoic acid ethyl ester 
• 140-88-5 ethyl acrylate 
• 64-17-5 ethanol 
• 141-82-2 malonic acid 
• 33745-47-0 3-formyl-benzoic acid ethyl ester 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Downstream Products

• 10036-23-4 3-<3-Ethoxycarbonyl-cyclohexyl>-propionsaeure-ethylester 

Relevant articles and documents

Phosphine-Catalyzed Anti -Hydroboration of Internal Alkynes

Trialkylphosphine organocatalysts have enabled regioselective anti-hydroboration of internal alkynes with pinacolborane reagents to provide (E)-disubstituted alkenylboronate compounds. The alkenylboronate can be used for derivatizations, such as protodebo

S,O-Ligand-Promoted Palladium-Catalyzed C-H Functionalization Reactions of Nondirected Arenes

Pd(II)-catalyzed C-H functionalization of nondirected arenes has been realized using an inexpensive and easily accessible type of bidentate S,O-ligand. The catalytic system shows high efficiency in the C-H olefination reaction of electron-rich and electron-poor arenes. This methodology is operationally simple, scalable, and can be used in late-stage functionalization of complex molecules. The broad applicability of this catalyst has been showcased in other transformations such as Pd(II)-catalyzed C-H acetoxylation and allylation reactions.