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6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid is a complex organic compound with a molecular formula of C20H22O8. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and features multiple hydroxyl, methoxy, and carboxyl functional groups. 6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid is characterized by its unique structure, which includes a tetrahydronapthalene core with various substituents, such as hydroxyl and methoxy groups, attached to different positions on the molecule. The presence of these functional groups and the compound's overall structure contribute to its potential applications in various fields, including pharmaceuticals and chemical research. Due to its complexity, 6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid may exhibit unique chemical properties and reactivity, making it an interesting subject for further study and potential development.

11041-15-9

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11041-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 11041-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,0,4 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 11041-15:
(7*1)+(6*1)+(5*0)+(4*4)+(3*1)+(2*1)+(1*5)=39
39 % 10 = 9
So 11041-15-9 is a valid CAS Registry Number.

11041-15-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:11041-15-9 SDS

11041-15-9Downstream Products

11041-15-9Relevant academic research and scientific papers

Gold particle size effect in biomass-derived lignan hydroxymatairesinol oxidation over Au/Al2O3 catalysts

López, Martín,Simakova, Olga A.,Murzina, Elena V.,Willf?r, Stefan M.,Prosvirin, Igor,Simakov, Andrey,Murzin, Dmitry Yu.

, p. 248 - 255 (2015/02/19)

The heterogeneously catalyzed aerobic selective oxidation of naturally occurring lignan hydroxymatairesinol (HMR) to another lignan oxomatairesinol (oxoMAT) was carried out at 70°C and atmospheric pressure over gold nanoparticles with different sizes supp

Oxidative dehydrogenation of a biomass derived lignan - Hydroxymatairesinol over heterogeneous gold catalysts

Simakova, Olga A.,Murzina, Elena V.,Maeki-Arvela, Paeivi,Leino, Anne-Riikka,Campo, Betiana C.,Kordas, Krisztian,Willfoer, Stefan M.,Salmi, Tapio,Murzin, Dmitry Yu.

experimental part, p. 54 - 64 (2011/09/20)

Synthesis of the lignan oxomatairesinol via oxidative dehydrogenation of the naturally occurring lignan hydroxymatairesinol was studied over gold catalysts supported on C, TiO2, SiO2, Al2O 3, and MgO. In order to investigate the reaction performance over the gold catalyst, synthesis of lignan oxomatairesinol was carried out in different organic solvents/water mixtures under synthetic air and nitrogen atmosphere at 373 K, and using also isolated hydroxymatairesinol isomers as a starting material. The results were compared with those obtained over palladium catalysts. Synthesized supported gold catalysts as well as the corresponding supports were characterized by TEM, XRD, ICP-OES, CO2-TPD, FTIR (using pyridine as a probe molecule), and XPS. Gold catalysts were shown to display superior performance compared with palladium ones: the activity was 4 times higher, with selectivity toward oxomatairesinol being 100%, while 60-85% were obtained over palladium catalysts. In contrast to palladium, the activity of gold catalysts is high in aerobic conditions and water-propan-2-ol mixture. However, activity and selectivity of gold catalysts were shown to be dependent on the electronic state of the metal and, similar to palladium catalysts, on the support acidity.

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