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(E)-5-phenylpent-4-en-2-yl 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1384458-53-0

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1384458-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384458-53-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,4,5 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1384458-53:
(9*1)+(8*3)+(7*8)+(6*4)+(5*4)+(4*5)+(3*8)+(2*5)+(1*3)=190
190 % 10 = 0
So 1384458-53-0 is a valid CAS Registry Number.

1384458-53-0Relevant academic research and scientific papers

VINYLOGOUS PHENETHYLAMINES AS NEUROTRANSMITTER RELEASERS

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Paragraph 00121; 00123, (2017/12/02)

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

The biogenic amine transporter activity of vinylogous amphetamine analogs

Decker, Ann M.,Partilla, John S.,Baumann, Michael H.,Rothman, Richard B.,Blough, Bruce E.

supporting information, p. 1657 - 1663 (2016/08/24)

A series of vinylogous amphetamine analogs was synthesized and examined for their activity at biogenic amine transporters and serotonin-2 receptor (5-HT2) subtypes. (1S,3E)-1-Methyl-4-phenyl-but-3-enylamine (S-6) is a potent dual dopamine/serotonin (DA/5-HT) releaser with no activity at 5-HT2 receptors. This unique profile of actions suggests that analog S-6 is a viable lead compound for identifying new structural classes of DA/5-HT releasers with therapeutic benefit and reduced abuse liability.

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

Stokes, Benjamin J.,Bischoff, Amanda J.,Sigman, Matthew S.

, p. 2336 - 2339 (2014/05/20)

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.

Palladium-catalyzed allylic cross-coupling reactions of primary and secondary homoallylic electrophiles

Stokes, Benjamin J.,Opra, Susanne M.,Sigman, Matthew S.

, p. 11408 - 11411 (2012/09/05)

The Pd(0)-catalyzed allylic cross-coupling of homoallylic tosylate substrates using boronic acids and pinacol esters is reported. The reaction uses 2-(4,5-dihydro-2-oxazolyl)quinoline (quinox) as a ligand and is performed at ambient temperature. The scope of the reaction is broad in terms of both the boronate transmetalating reagent and the substrate and includes secondary tosylates. Mechanistic studies support an alkene-mediated SN2-type stereoinvertive oxidative addition of unactivated primary and secondary alkyl tosylates.

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