1384458-53-0

Basic information

• Product Name: (E)-5-phenylpent-4-en-2-yl 4-methylbenzenesulfonate
• Synonyms: (E)-5-phenylpent-4-en-2-yl 4-methylbenzenesulfonate
• CAS NO: 1384458-53-0
• Molecular Weight: 316.421
• Mol File: 1384458-53-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-5-phenylpent-4-en-2-yl 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-5-phenylpent-4-en-2-yl 4-methylbenzenesulfonate(1384458-53-0)
• EPA Substance Registry System: (E)-5-phenylpent-4-en-2-yl 4-methylbenzenesulfonate(1384458-53-0)

Safety Data

• Hazardous Substances Data: 1384458-53-0(Hazardous Substances Data)

Upstream product

• 54985-34-1 trans-1-phenyl-1-penten-3-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 16330-23-7 1-phenyl-1-pentyn-4-ol 
• 100-42-5 styrene 
• 52753-86-3 pent-4-en-2-yl 4-methylbenzenesulfonate 
• 98-80-6 phenylboronic acid 

Downstream Products

• 189322-54-1 (E)-pent-1-ene-1,3-diyldibenzene 
• 1236889-51-2 C₁₈H₂₀O 
• 1357175-54-2 (E)-3-(4-chloropheny)-1-phenylpent-1-ene 

Relevant articles and documents

VINYLOGOUS PHENETHYLAMINES AS NEUROTRANSMITTER RELEASERS

The disclosure provides monoamine neurotransmitter releaser and/or monoamine uptake inhibitor compounds having biogenic amine transporter activity but lacking substantial activity at 5-HT2 receptor subtypes. The phenethylamine or vinylogous phe

Pd(quinox)-catalyzed allylic relay Suzuki reactions of secondary homostyrenyl tosylates via alkene-assisted oxidative addition

Pd-catalyzed allylic relay Suzuki cross-coupling reactions of secondary alkyl tosylates, featuring a sterically-hindered oxidative addition and precise control of β-hydride elimination, are reported. The identification of a linear free energy relationship between the relative rates of substrate consumption and the electronic nature of the substrate alkene suggests that the oxidative addition requires direct alkene involvement. A study of the effect of alkyl chain length on the reaction outcome supports a chelation-controlled oxidative addition. This journal is the Partner Organisations 2014.