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(E)-3-(prop-1-en-1-yl)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66921-90-2

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66921-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66921-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,2 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66921-90:
(7*6)+(6*6)+(5*9)+(4*2)+(3*1)+(2*9)+(1*0)=152
152 % 10 = 2
So 66921-90-2 is a valid CAS Registry Number.

66921-90-2Relevant academic research and scientific papers

Iron-catalyzed decarboxylative methylation of α,β-unsaturated acids under ligand-free conditions

Rong, Guangwei,Liu, Defu,Lu, Linhua,Yan, Hong,Zheng, Yang,Chen, Jie,Mao, Jincheng

, p. 5033 - 5037 (2014/07/08)

It is the first time to find that iron-catalyzed decarboxylative methylation of α,β-unsaturated acids could be performed in the absence of any ligands. During the reaction, the configuration of the double bond could be retained. It is noteworthy that di-t

Iron-catalyzed decarboxylative methylation of α,β-unsaturated acids under ligand-free conditions

Rong, Guangwei,Liu, Defu,Lu, Linhua,Yan, Hong,Zheng, Yang,Chen, Jie,Mao, Jincheng

, p. 5033 - 5037 (2014/12/10)

It is the first time to find that iron-catalyzed decarboxylative methylation of α,β-unsaturated acids could be performed in the absence of any ligands. During the reaction, the configuration of the double bond could be retained. It is noteworthy that di-t

Expanding the regioselective enzymatic repertoire: Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta

Paul, Caroline E.,Rajagopalan, Aashrita,Lavandera, Ivan,Gotor-Fernandez, Vicente,Kroutil, Wolfgang,Gotor, Vicente

supporting information; experimental part, p. 3303 - 3305 (2012/04/23)

The first report of a biocatalytic regioselective oxidative mono-cleavage of dialkenes was successfully achieved employing a cell-free enzyme preparation from Trametes hirsuta at the expense of molecular oxygen. Selected reactions were performed on a preparative scale affording high to excellent conversions and chemoselectivities. The Royal Society of Chemistry 2012.

STRUCTURE-ACTIVITY RELATIONSHIPS OF PHENYLPROPANOIDS AS GROWTH INHIBITORS OF THE GREEN ALGA SELENASTRUM CAPRICORNUTUM

Greca, Marina Della,Monaco, Pietro,Pollio, Antonino,Previtera, Lucio

, p. 4119 - 4124 (2007/10/02)

Twenty-seven commercial or synthetic phenylpropanoids have been tested in broth against the unicellular alga Selenastrum capricornutum.The antialgal activity seems to be linked to the number as well as to the position of the methoxyl group in the molecule.A slight effect of the side chain substitution was also observed. Key Word Index - Selenastrum capricornutum; allelochemicals; phenylpropanoids.

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