3233-58-7 Usage
Uses
Used in Organic Synthesis:
Sulfuric acid, mono(4-methylphenyl) ester is used as a catalyst in organic synthesis for its ability to facilitate a wide range of chemical reactions, including esterification, hydrolysis, and condensation reactions. Its strong acidic properties enable it to act as an effective catalyst, improving the efficiency and selectivity of the reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, sulfuric acid, mono(4-methylphenyl) ester is used as a reagent in the manufacture of various drugs. Its acidic nature allows it to participate in the synthesis of active pharmaceutical ingredients, contributing to the development of new medications.
Used in Dye Production:
Sulfuric acid, mono(4-methylphenyl) ester is utilized in the production of dyes due to its ability to act as a catalyst in dye synthesis. Its strong acidity aids in the formation of dye molecules, enhancing the color intensity and stability of the final product.
Used in Pesticide Manufacturing:
In the agricultural sector, sulfuric acid, mono(4-methylphenyl) ester is employed in the manufacturing process of pesticides. Its acidic properties play a crucial role in the synthesis of active ingredients, ensuring the effectiveness of these products in controlling pests and diseases.
Used in Plastics, Resins, and Polymers Production:
Sulfuric acid, mono(4-methylphenyl) ester is also used in the production of plastics, resins, and polymers. Its strong acidic nature aids in the polymerization process, contributing to the formation of polymer chains and the development of various plastic materials with specific properties.
Due to the strong acidic nature of sulfuric acid, mono(4-methylphenyl) ester, it is essential to handle and use it with care, following proper safety precautions to prevent any potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 3233-58-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,3 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3233-58:
(6*3)+(5*2)+(4*3)+(3*3)+(2*5)+(1*8)=67
67 % 10 = 7
So 3233-58-7 is a valid CAS Registry Number.
3233-58-7Relevant academic research and scientific papers
Cho, Joo-Youn,Matsubara, Tsutomu,Kang, Dong Wook,Ahn, Sung-Hoon,Krausz, Kristopher W.,Idle, Jeffrey R.,Luecke, Hans,Gonzalez, Frank J.
, p. 1063 - 1074 (2010)
Farnesoid X receptor (FXR) is a nuclear receptor that regulates genes involved in synthesis, metabolism, and transport of bile acids and thus plays a major role in maintaining bile acid homeostasis. In this study, metabolomic responses were investigated in urine of wild-type and Fxr-null mice fed cholic acid, an FXR ligand, using ultra-performance liquid chromatography (UPLC) coupled with electrospray time-of-flight mass spectrometry (TOFMS). Multivariate data analysis between wild-type and Fxr-null mice on a cholic acid diet revealed that the most increased ions were metabolites of p-cresol (4-methylphenol), corticosterone, and cholic acid in Fxr-null mice. The structural identities of the above metabolites were confirmed by chemical synthesis and by comparing retention time (RT) and/or tandem mass fragmentation patterns of the urinary metabolites with the authentic standards. Tauro-3α,6,7α,12α-tetrol (3α,6,7α,12α- tetrahydroxy-5β-cholestan-26-oyltaurine), one of the most increased metabolites in Fxr-null mice on a CA diet, is a marker for efficient hydroxylation of toxic bile acids possibly through induction of Cyp3a11. A cholestatic model induced by lithocholic acid revealed that enhanced expression of Cyp3a11 is the major defense mechanism to detoxify cholestatic bile acids in Fxr-null mice. These results will be useful for identification of biomarkers for cholestasis and for determination of adaptive molecular mechanisms in cholestasis.
