26429-97-0

Basic information

• Product Name: (2E)-5-Phenyl-2-pentenoic acid methyl ester
• Synonyms: (2E)-5-Phenyl-2-pentenoic acid methyl ester;(E)-5-Phenyl-2-pentenoic acid methyl ester
• CAS NO: 26429-97-0
• Molecular Formula: C₁₂H₁₄O₂
• Molecular Weight: 190.24
• Mol File: 26429-97-0.mol
• Article Data: 40

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2E)-5-Phenyl-2-pentenoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-5-Phenyl-2-pentenoic acid methyl ester(26429-97-0)
• EPA Substance Registry System: (2E)-5-Phenyl-2-pentenoic acid methyl ester(26429-97-0)

Safety Data

• Hazardous Substances Data: 26429-97-0(Hazardous Substances Data)

Upstream product

• 40467-01-4 methyl(triphenylphosphoranylidene)acetate 
• 104-53-0 3-phenyl-propionaldehyde 
• 96-32-2 bromoacetic acid methyl ester 
• 5927-18-4 trimethyl phosphonoacetate 
• 18328-11-5 3-benzyl propionaldehyde 
• 67-56-1 methanol 
• 24271-22-5 5-phenyl-2(E)-pentenoic acid 
• 100-52-7 benzaldehyde 
• 140-10-3 (E)-3-phenylacrylic acid 
• 1067-74-9 Methyl diethylphosphonoacetate 
• 186581-53-3 diazomethane 
• 122-97-4 3-Phenyl-1-propanol 
• 65-85-0 benzoic acid 
• 768-56-9 4-Phenylbut-1-ene 

Downstream Products

• 33046-84-3 (2E)-5-phenyl-2-pentenal 
• 112606-95-8 5-(1-phenylethyl)-2-tetrahydrofuranone 
• 126175-28-8 methyl 4-(N,N'-bis(ethoxycarbonyl)hydrazino)-5-phenyl-2-pentenoate 
• 117213-94-2 3-Phenethyl-pentanedioic acid dimethyl ester 
• 20620-59-1 5-phenyl-n-valeric acid methyl ester 

Relevant articles and documents

Ligand-controlled cobalt-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes

The Co-catalyzed remote hydroboration and alkene isomerization of allylic siloxanes were realized by a ligand-controlled strategy. The remote hydroboration with dcype provided borylethers, while xantphos favored the formation of silyl enol ethers.

Trifluoromethylation of Unactivated Alkenes with Me3SiCF3 and N-Iodosuccinimide

A novel approach to the trifluoromethylation of unactivated alkenes is presented. This reaction is promoted by N-iodosuccinimide (NIS) under visible light irradiation without the need for photocatalysts. The mild conditions allow the direct synthesis of u

Formation of Enol Ethers by Radical Decarboxylation of α-Alkoxy β-Phenylthio Acids

Enol ethers are formed by radical decarboxylation of α-alkoxy β-phenylthio acids via the corresponding Barton esters. The phenylthio acids were usually made by the known regioselective reaction of α,β-epoxy acids with PhSH in the presence of InCl3, followed by O-alkylation of the resulting alcohol. In one case, thiol addition to an α,β-unsaturated ethoxymethyl ester was used.