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(+/-)-Z-2-methyl-1,3-bis(4-methoxyphenyl)pent-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79091-05-7

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79091-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79091-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,9 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79091-05:
(7*7)+(6*9)+(5*0)+(4*9)+(3*1)+(2*0)+(1*5)=147
147 % 10 = 7
So 79091-05-7 is a valid CAS Registry Number.

79091-05-7Downstream Products

79091-05-7Relevant academic research and scientific papers

Carbenium ions generated upon adsorption of 4-methoxystyrenes onto acid zeolites. A kinetic study

Fornes, Vicente,Garcia, Hermenegildo,Marti, Vicente,Fernandez, Lorenzo

, p. 3827 - 3832 (1998)

Adsorption of vinylanisole and trans-(4-methoxyphenyl)-1-propene into HY, Hβ and HZSM-5 allows us to detect the corresponding substituted 1,3- bis(4-methoxyphenyl)-1-propylium (2), 1-(4-methoxyphenyl)-6-methoxy-1- indanylium (5) and 1,3-bis(4-methoxyphenyl)-2-propen-1-ylium (8) cations as reactive intermediates. The kinetics can be followed by conventional spectrophotometers. Cation 2 appears as the shorter lived species, decaying in hours for the HY sample and within days when embedded in HZSM-5 zeolite. Cyclic indanyl cation 5 shows a-lifetime much longer than 2. A growth of 8 concomitantly with the decay of 2 has been also observed. This has been taken as a proof of a hydride transfer from neutral 1,3-bis(4-methoxyphenyl)-1- propenes (the corresponding acyclic dimers observed as products) as donors to cations 2 as acceptors leading to 8.

Anomalous behaviour of Pd(II) on phenylpropanoids

Thappa,Agarwal,Dhar

, p. 731 - 733 (2007/10/03)

Exposure of phenylpropanoids like methyleugenol, eugenol and methylchavicol to Pd(II) chloride in acetic acid results in α,β linked unsymmetrical dimers. Dimeric coupling is characteristic of phenylpropanoids whereas cyclisation to indanes require the pre

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