85969-93-3

Basic information

• Product Name: potassium 2-benzyl-3-ethoxy-3-oxopropanoate
• Synonyms: potassium 2-benzyl-3-ethoxy-3-oxopropanoate
• CAS NO: 85969-93-3
• Molecular Weight: 260.331
• Mol File: 85969-93-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: potassium 2-benzyl-3-ethoxy-3-oxopropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: potassium 2-benzyl-3-ethoxy-3-oxopropanoate(85969-93-3)
• EPA Substance Registry System: potassium 2-benzyl-3-ethoxy-3-oxopropanoate(85969-93-3)

Safety Data

• Hazardous Substances Data: 85969-93-3(Hazardous Substances Data)

Upstream product

• 607-81-8 diethyl 2-benzylmalonate 

Downstream Products

• 78551-75-4 2-Benzyl-2-bromo-malonic acid monoethyl ester 
• 726194-05-4 2,3,4-tribenzyl-γ-butyro-2-en-lactone 
• 101308-40-1 ethyl 2-bromo-3-phenylpropionate 
• 103-36-6 ethyl 3-phenyl-2-propenoate 
• 133472-43-2 ethyl 4-(1-acetoxyisopropyl)-3-benzyl-2-oxotetrahydrofuran-3-carboxylate 
• 133472-42-1 ethyl 3-benzyl-4-isopropenyl-2-oxotetrahydrofuran-3-carboxylate 
• 133472-35-2 1-benzyl-4,4-dimethyl-3,7-dioxabicyclo<3.3.0>octane-2,8-dione 
• 74106-38-0 1-benzyl-3,7-dioxabicyclo<3.3.0>octane-2,8-dione 
• 1026045-48-6 2-Benzyl-N-benzyloxy-N'-[(S)-3-phenyl-1-(2-p-tolyl-ethylcarbamoyl)-propyl]-malonamide 
• 1026887-20-6 2-Benzyl-N-benzyloxy-N'-(3-phenyl-propyl)-malonamide 
• 1026913-20-1 2-Benzyl-N-benzyloxy-3-morpholin-4-yl-3-oxo-propionamide 
• 67681-99-6 α-[(benzyloxy)carbamoyl]hydrocinnamic acid 
• 67681-98-5 2(RS)-{[(benzyloxy)amino]carbonyl}-3-phenylpropanoic acid ethyl ester 
• 133472-28-3 ethyl 2-propenyl 2-benzylpropanedioate 

Relevant articles and documents

Synthesis of maculalactone A and derivatives for environmental fate tracking studies

Maculalactone A (1) constitutes a promising antifouling agent, inhibiting the formation of biofilms in marine and freshwater systems. In this study, we developed a new route, based on a late-stage formation of the butenolide core, leading to the total synthesis of maculalactone A (three steps, overall yield of 45%) and delivering material on a gram scale. In addition, analogues of the title compound were assayed concerning their biological activity, utilizing Artemia franciscana and Thamnocephalus platyurus. The most active analogue was functionalized with a rhodamine B fluorophore and was utilized in an in vivo staining experiment in Artemia salina. Two different tissues were found to accumulate this maculalactone A derivative. This journal is