128839-49-6

Basic information

• Product Name: methyl (Z)-2-(pent-1-en-1-yl)benzoate
• Synonyms: methyl (Z)-2-(pent-1-en-1-yl)benzoate
• CAS NO: 128839-49-6
• Molecular Weight: 204.269
• Mol File: 128839-49-6.mol

Chemical Properties

• CAS DataBase Reference: methyl (Z)-2-(pent-1-en-1-yl)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (Z)-2-(pent-1-en-1-yl)benzoate(128839-49-6)
• EPA Substance Registry System: methyl (Z)-2-(pent-1-en-1-yl)benzoate(128839-49-6)

Safety Data

• Hazardous Substances Data: 128839-49-6(Hazardous Substances Data)

Upstream product

• 60494-73-7 (2-methoxycarbonylbenzyl)triphenylphosphonium bromide 
• 123-72-8 butyraldehyde 
• 3728-50-5 butylidenetriphenylphosphorane 
• 4122-56-9 methyl o-formylbenzoate 
• 1779-51-7 n-butyl(triphenyl)phosphonium bromide 
• 119-67-5 o-carboxybenzaldehyde 

Downstream Products

• 128839-50-9 2-(1-Z-pentenyl)benzyl alcohol 
• 125775-13-5 3-(2-(1-Z-n-pentenyl)phenyl)-E-acrylic acid 
• 220903-35-5 (Z)-2-(pent-1-en-1-yl)benzaldehyde 
• 220903-36-6 3-(2-(1-Z-pentenyl)phenyl)-E-acrylic acid hydroxyazo benzotriazolyl ester 
• 147317-36-0 pepticinnamin E 
• 147317-36-0 epi-pepticinnamin E 

Relevant articles and documents

An Easy-to-Machine Electrochemical Flow Microreactor: Efficient Synthesis of Isoindolinone and Flow Functionalization

Flow electrochemistry is an efficient methodology to generate radical intermediates. An electrochemical flow microreactor has been designed and manufactured to improve the efficiency of electrochemical flow reactions. With this device only little or no supporting electrolytes are needed, making processes less costly and enabling easier purification. This is demonstrated by the facile synthesis of amidyl radicals used in intramolecular hydroaminations to produce isoindolinones. The combination with inline mass spectrometry facilitates a much easier combination of chemical steps in a single flow process.

Synthesis and in vitro evaluation of the farnesyltransferase inhibitor pepticinnamin E

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Palladium-Assisted (Z)-(E) Isomerization of Styrenes

It is shown that treatment of stereoisomeric mixtures of styrenes with a catalytic amount of bis(acetonitrile)dichloropalladium(II) achieves smooth stereoisomerization of the (Z)-isomers to the (E)-isomers.