1261280-45-8

Basic information

• Product Name: 5-(4-methoxyphenyl)hex-5-enoic acid methyl ester
• Synonyms: 5-(4-methoxyphenyl)hex-5-enoic acid methyl ester
• CAS NO: 1261280-45-8
• Molecular Weight: 234.295
• Mol File: 1261280-45-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-(4-methoxyphenyl)hex-5-enoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-methoxyphenyl)hex-5-enoic acid methyl ester(1261280-45-8)
• EPA Substance Registry System: 5-(4-methoxyphenyl)hex-5-enoic acid methyl ester(1261280-45-8)

Safety Data

• Hazardous Substances Data: 1261280-45-8(Hazardous Substances Data)

Upstream product

• 5720-07-0 4-methoxyphenylboronic acid 
• 77758-51-1 methyl hex-5-ynoate 
• 1847-68-3 5-(4-methoxy-phenyl)-5-oxo-pentanoic acid methyl ester 
• 6399-81-1 triphenylphosphine hydrobromide 
• 40949-94-8 potassium hexamethylsilazane 
• 4609-10-3 5-(4-methoxyphenyl)-5-oxopentanoic acid 
• 1779-49-3 Methyltriphenylphosphonium bromide 

Downstream Products

• 1258204-03-3 5-(4-methoxyphenyl)hex-5-enoic acid 
• 1258203-95-0 (S)-6-(iodomethyl)-6-(4-methoxyphenyl)tetrahydro-2H-pyran-2-one 
• 1370729-72-8 (R)-6-(iodomethyl)-6-(4-methoxyphenyl)tetrahydro-2H-pyran-2-one 

Relevant articles and documents

Enantioselective Organocatalyzed Bromolactonizations: Applications in Natural Product Synthesis

Asymmetric bromolactonization reactions of δ-unsaturated carboxylic acids have been investigated in the presence of 10 chiral squaramide hydrogen-bonding organocatalysts. The best catalyst enabled the cyclization of several 5-arylhex-5-enoic acids into th

Asymmetric bromolactonization catalyzed by a C3-symmetric chiral trisimidazoline

A productive alliance: In an enantioselective organocatalytic bromolactonization of 5-substituted hex-5-enoic acids (see scheme), it appears that the formation of an ion pair through interaction of the trisimidazoline catalyst 1 with the substrate both cr