13152-95-9 Usage
Uses
Used in Pharmaceutical Research:
(2,4-dimethylphenyl)(3-methylphenyl)methanone is used as a building block for the development of pharmaceuticals due to its potential to be incorporated into more complex molecular structures that can exhibit therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, (2,4-dimethylphenyl)(3-methylphenyl)methanone is used as a starting material for synthesizing various agrochemicals, contributing to the development of pesticides and other agricultural products.
Used in Specialty Chemicals:
(2,4-dimethylphenyl)(3-methylphenyl)methanone is employed in the production of specialty chemicals, where its unique structure and properties can be leveraged to create specific compounds for various applications.
Used in Fragrance Production:
(2,4-dimethylphenyl)(3-methylphenyl)methanone may also be used in the fragrance industry, where its aromatic properties can be utilized to develop unique scents for perfumes, cosmetics, and other scented products.
Used in Dye Manufacturing:
(2,4-dimethylphenyl)(3-methylphenyl)methanone can be used in the dye industry for the production of dyes, taking advantage of its chemical structure to create dyes with specific color characteristics and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 13152-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13152-95:
(7*1)+(6*3)+(5*1)+(4*5)+(3*2)+(2*9)+(1*5)=79
79 % 10 = 9
So 13152-95-9 is a valid CAS Registry Number.
13152-95-9Relevant academic research and scientific papers
Class of Friedel-crafts catalysts
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, (2008/06/13)
Molybdenum compounds, particularly molybdenum sulfide, molybdenum silicide, molybdenum selenide and molybdenum telluride are useful Friedel-Crafts catalysts for the aralkylation of aromatics to produce polybenzyls, the manufacture of aromatic ketones, aromatic sulfones and aromatic esters. The foregoing processes are carried out at a temperature of about 60° to 250° C. and at a catalyst concentration of about 0.1 to 15% by weight of reactants. The reaction products are useful as laminates, herbicides and bactericides.
