40203-51-8

Basic information

• Product Name: 2-Propenoic acid, 3-methoxy-3-phenyl-, methyl ester, (Z)-
• CAS NO: 40203-51-8
• Molecular Formula: C11H12O3
• Molecular Weight: 192.214
• Mol File: 40203-51-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-methoxy-3-phenyl-, methyl ester, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-methoxy-3-phenyl-, methyl ester, (Z)-(40203-51-8)
• EPA Substance Registry System: 2-Propenoic acid, 3-methoxy-3-phenyl-, methyl ester, (Z)-(40203-51-8)

Safety Data

• Hazardous Substances Data: 40203-51-8(Hazardous Substances Data)

Upstream product

• 614-27-7 methyl 3-oxo-3-phenylpropionate 
• 614-16-4 Benzoylacetonitrile 
• 536-74-3 phenylacetylene 
• 616-38-6 carbonic acid dimethyl ester 
• 37823-96-4 pentacarbonyl(methoxyphenylmethylene)tungsten⁽⁰⁾ 
• 383-72-2 N-(trifluoroacetyl)glycine methyl ester 
• 532-27-4 1-chloroacetophenone 

Downstream Products

• 868280-59-5 5-phenyl-2-pyridin-2-ylpyrimidin-4-ol 

Relevant articles and documents

Alkoxide-catalyzed addition of alkyl carbonates across alkynes-stereoselective synthesis of (: E)-β-alkoxyacrylates

Dialkyl carbonates were found to regio- and stereoselectively add to terminal alkynes in the presence of catalytic amounts of potassium methoxide. Various synthetically meaningful aryl- and heteroaryl-substituted (E)-β-alkoxyacrylates were thus obtained i

A simple and efficient transformation of fischer carbene complexes into bromomethyl ketones or β-ketoesters

Fischer-type carbene complexes react via nucleophilic attack with dibromomethyllithium or haloester lithium enolates to afford bromomethyl ketones or β-ketoesters, respectively.