910661-38-0

Basic information

• Product Name: ethyl (E)-3-(3-methyl-2-(3-oxobutyl)phenyl)acrylate
• Synonyms: ethyl (E)-3-(3-methyl-2-(3-oxobutyl)phenyl)acrylate
• CAS NO: 910661-38-0
• Molecular Weight: 246.306
• Mol File: 910661-38-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl (E)-3-(3-methyl-2-(3-oxobutyl)phenyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (E)-3-(3-methyl-2-(3-oxobutyl)phenyl)acrylate(910661-38-0)
• EPA Substance Registry System: ethyl (E)-3-(3-methyl-2-(3-oxobutyl)phenyl)acrylate(910661-38-0)

Safety Data

• Hazardous Substances Data: 910661-38-0(Hazardous Substances Data)

Upstream product

• 2550-26-7 4-Phenyl-2-butanone 
• 140-88-5 ethyl acrylate 
• 91047-77-7 ethyl (2E)-3-(2-bromophenyl)prop-2-enoate 
• 78-94-4 methyl vinyl ketone 

Downstream Products

• 910661-55-1 3-[2-(3-hydroxybutyl)phenyl]propanoic acid 
• 910661-49-3 ethyl 3-[2-(3-hydroxybutyl)phenyl]propanoate 

Relevant articles and documents

Pd(II)-Catalyzed C-H Functionalizations Directed by Distal Weakly Coordinating Functional Groups

Ortho-C(sp2)-H olefination and acetoxylation of broadly useful synthetic building blocks phenylacetyl Weinreb amides, esters, and ketones are developed without installing an additional directing group. The interplay between the distal weak coor

Access to a new family of medium ring aromatic lactones

We report a new method for preparation of hydroxyacids as precursors of benzolactones using a simple and an efficient electrochemical step. This gives in only four steps six- to eleven-membered lactones with high isolated yields from conveniently substituted aryl bromides. The lactonisation was performed according to the Yamamoto's process.