5724-05-0

Basic information

• Product Name: 5-(p-tolyl)pent-4-enoic acid
• Synonyms: 5-(p-tolyl)pent-4-enoic acid
• CAS NO: 5724-05-0
• Molecular Weight: 190.242
• Mol File: 5724-05-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 5-(p-tolyl)pent-4-enoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(p-tolyl)pent-4-enoic acid(5724-05-0)
• EPA Substance Registry System: 5-(p-tolyl)pent-4-enoic acid(5724-05-0)

Safety Data

• Hazardous Substances Data: 5724-05-0(Hazardous Substances Data)

Upstream product

• 622-97-9 1-ethenyl-4-methylbenzene 
• 591-80-0 pent-4-enoic acid 
• 54636-56-5 (E)-1-(3-bromoprop-1-en-1-yl)-4-methylbenzene 
• 122058-30-4 p-methylcinnamyl alcohol 
• 97585-04-1 ethyl (E)-3-(4-methylphenyl)acrylate 
• 104-87-0 4-methyl-benzaldehyde 
• 624-31-7 4-tolyl iodide 
• 603-35-0 triphenylphosphine 
• 17857-14-6 (3-carboxypropyl)(triphenyl)phosphonium bromide 
• 124-38-9 carbon dioxide 
• 55088-80-7 1-(cyclopropylidenemethyl)-4-methylbenzene 

Downstream Products

• 1300698-88-7 (5R,6S)-5-bromo-6-p-tolyltetrahydro-2H-pyran-2-one 
• 420119-86-4 (+/-)-5-(4-methylphenylcarbonyl)dihydrofuran-2(3H)-one 
• 100388-65-6 5-(p-tolyl)pentanoyl chloride 
• 777-93-5 5-(p-tolyl)pentanoic acid 
• 1322547-44-3 1-{5-[(1S,3R)-3-amino-3-(hydroxymethyl)cyclopentyl]-1-methyl-1H-pyrrol-2-yl}-5-(4-methylphenyl)pentan-1-one 
• 1431329-93-9 tert-butyl (5R,7S)-2,2-dimethyl-7-{1-methyl-5-[5-(4-methylphenyl)pentanoyl]-1H-pyrrol-2-yl}-3-oxa-1-azaspiro[4.4]nonane-1-carboxylate 
• 1431329-92-8 C₄₃H₅₈N₂O₅ 
• 1380523-51-2 (E)-5-p-tolylpent-4-enyl methanesulfonate 
• 76978-38-6 (E)-5-(4-methylphenyl)-4-penten-1-ol 
• 1351858-73-5 (2R)-tetrahydro-2-[(S)-bromo(4-methylphenyl)methyl]furan 
• 1351858-83-7 (2R,3S)-3-bromotetrahydro-2-(4-methylphenyl)-2H-pyran 
• 5724-00-5 Bis-<4-(4-methyl-benzyliden)-butyryl>-peroxid 

Relevant articles and documents

Synthesis of Antitricyclic Morpholine Derivatives through Iodine(III)-Mediated Intramolecular Umpolung Cycloaddition of Olefins

A (diacetoxyiodo)benzene-mediated intramolecular cycloaddition of olefins to construct tricyclic morpholines is presented. A series of substituted tricyclic morpholines were obtained in one-step simple operation under mild conditions, and the NMR studies

trans-Cyclooctenes as Halolactonization Catalysts

The strained olefins in trans-cyclooctenes serve as efficient catalysts for halolactonizations, including bromolactonizations and iodolactonizations. The trans-cyclooctene framework is essential for excellent catalytic performance, and the substituents also play important roles in determining efficiency. These results are the first demonstration of catalysis by a trans-cyclooctene.

Aminothiocarbamate-catalyzed asymmetric bromolactonization of 1,2-disubstituted olefinic acids

An efficient and enantioselective bromolactonization of 1,2-disubstituted olefinic acids using an amino-thiocarbamate catalyst has been developed, resulting in the formation of δ-lactones containing two chiral centers with up to 99% yield, 95% ee.