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2,2',6,6'-Tetramethoxy-azobenzol is a synthetic organic compound characterized by its azobenzene structure, which a features diazo group (-N=N-) connecting two aromatic rings. This particular compound is distinguished by the presence of four methoxy groups (-OCH3), which are attached to the 2, 2', 6, and 6' positions of the benzene rings. The methoxy groups contribute to the compound's solubility and stability. Azobenzene compounds are known for their photoisomerization properties, where they can switch between trans and cis isomers upon exposure to light, making them useful in various applications such as in the production of photochromic materials, liquid crystals, and as components in chemical reactions that involve light-induced changes. The specific arrangement of the methoxy groups in 2,2',6,6'-Tetramethoxy-azobenzol influences its electronic properties and reactivity, potentially affecting its use in specific industrial or research applications.

29418-56-2

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29418-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29418-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,1 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29418-56:
(7*2)+(6*9)+(5*4)+(4*1)+(3*8)+(2*5)+(1*6)=132
132 % 10 = 2
So 29418-56-2 is a valid CAS Registry Number.

29418-56-2Upstream product

29418-56-2Downstream Products

29418-56-2Relevant academic research and scientific papers

Oxidation of some methoxy anilines by tetrabutylammoniumbromochromate in aqueous acetic acid medium: A kinetics study

Jabir, Shaik,Asghar, Basim H.,Mansoor, S. Sheik

, p. 1806 - 1810 (2017)

The oxidation of aniline (A), 2,4-dimethoxy aniline (2,4-DMA), 2,6-dimethoxy aniline (2,6-DMA), 2,4,6-trimethoxy aniline (2,4,6-TMA) and 3,4,5-trimethoxy aniline (3,4,5-TMA) by tetrabutylammoniumbromochromate (TBABC) have been studied in 50 % acetic acid – 50 % water medium in the presence of perchloric acid. The oxidation leads to the formation of the corresponding azobenzenes. The reaction is first order with respect to [TBABC], [S] and [H+]. The reaction has been found to be catalyzed by H+ ions. The reactions were studied at four different temperatures and thermodynamic parameters were calculated. The rates decreased in the order: 2,4,6-TMA > 2,6-DMA > 2,4-DMA > 3,4,5-TMA > aniline.

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