525-52-0 Usage
Description
1,2,3-Triacetoxybenzene, also known as triacetoxybenzol, is an organic compound with the chemical formula C10H10O5. It is a colorless crystalline solid that is soluble in organic solvents. The molecule consists of a benzene ring with three acetoxy groups attached to it, which gives it unique chemical properties and reactivity.
Uses
Used in Photography:
1,2,3-Triacetoxybenzene is used as a developer in photography for the processing of photographic films and papers. Its reducing properties enable the conversion of silver ions into metallic silver, which forms the image on the film or paper.
Used in Colloidal Solutions:
1,2,3-Triacetoxybenzene is used in the preparation of colloidal solutions of metals, such as gold and silver. 1,2,3-TRIACETOXYBENZENE acts as a reducing agent, allowing the formation of stable colloidal particles of the metal.
Used in Textile Industry:
1,2,3-Triacetoxybenzene is used as a mordant for wool, which helps to fix dyes to the fiber and improve the colorfastness of the dyed material. It is also used in the staining of leather and the process of engraving.
Used in Dye Manufacturing:
1,2,3-Triacetoxybenzene is used in the manufacture of various dyes, including those used for dyeing furs, hair, and other materials. Its reactivity with other chemicals allows for the synthesis of a wide range of dye compounds.
Used in Analytical Chemistry:
1,2,3-Triacetoxybenzene is used as a reagent in analytical chemistry for the detection and analysis of antimony and bismuth. Its reducing properties enable the formation of colored complexes with these elements, which can be used for their identification and quantification.
Used as an Active Reducer:
1,2,3-Triacetoxybenzene is used as an active reducer for gold, silver, and mercury salts. Its reducing properties allow for the conversion of these metal ions into their elemental forms, which can be useful in various chemical processes and applications.
Used in Gas Analysis:
1,2,3-Triacetoxybenzene is used for the absorption of oxygen in gas analysis. Its ability to react with oxygen allows for the accurate measurement of oxygen levels in various gas mixtures, which is important in fields such as environmental monitoring and industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 525-52-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 525-52:
(5*5)+(4*2)+(3*5)+(2*5)+(1*2)=60
60 % 10 = 0
So 525-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O6/c1-7(13)16-10-5-4-6-11(17-8(2)14)12(10)18-9(3)15/h4-6H,1-3H3
525-52-0Relevant articles and documents
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Billek,G. et al.
, p. 909 - 915 (1962)
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An efficient method to prepare aryl acetates by the carbonylation of aryl methyl ethers or phenols
Zhang, Dejin,Yang, Guoqiang,Xiong, Junping,Liu, Jia,Hu, Xingbang,Zhang, Zhibing
, p. 2683 - 2687 (2021/02/16)
Synthesis of valuable chemicals from lignin based compounds is critical for the application of biomass. Here, we develop a method of preparing aryl acetates by the carbonylation of aryl methyl ethers or phenols under low CO pressure. Good to excellent yields of aryl acetates were obtained using different substrates, and a possible reaction mechanism was proposed by conducting a series of control experiments. This method may provide a potential way for the utilization of lignin.
Highly efficient and recyclable acetylation of phenols and alcohols by nickel zirconium phosphate under solvent-free conditions
Hajipour, Abdol Reza,Karimi, Hirbod,Kohi, Afshin
, p. 55 - 64 (2016/01/09)
Nickel zirconium phosphate nanoparticles have been used as an efficient catalyst for the acetylation of a wide range of alcohols and phenols with acetic anhydride in good to excellent yields under solvent-free conditions. The steric and electronic properties of the different substrates had a significant influence on the reaction conditions required to achieve the acetylation. The catalyst used in the current study was characterized by inductively coupled plasma optical emission spectroscopy, X-ray diffraction, N2 adsorption-desorption, scanning electron microscopy, and transmission electron microscopy. This nanocatalyst could also be recovered and reused at least six times without any discernible decrease in its catalytic activity.
