5335-24-0 Usage
Uses
Used in Personal Care Products:
4,6-Dichloro-2-phenylphenol is used as a preservative in personal care products for its ability to inhibit the growth of microorganisms, thereby extending the shelf life and maintaining the quality of these products.
Used in Pharmaceuticals:
In the pharmaceutical industry, 4,6-Dichloro-2-phenylphenol is utilized as a preservative to prevent microbial contamination in various formulations, ensuring the safety and efficacy of the products.
Used in Industrial Applications:
4,6-Dichloro-2-phenylphenol is used as a fungicide and bactericide in industrial settings, particularly for the preservation of cutting fluids, which helps to prevent the growth of microorganisms that can cause spoilage and degradation.
Used in Household Disinfectants:
4,6-Dichloro-2-phenylphenol is employed in the formulation of household disinfectants, where it serves to eliminate harmful microorganisms and maintain a hygienic environment.
Used in Textile and Leather Industries:
4,6-Dichloro-2-phenylphenol is used in the textile and leather industries to control mold and mildew, preserving the quality and appearance of these materials over time.
However, due to potential toxicity and environmental concerns, there are restrictions on the use of 4,6-Dichloro-2-phenylphenol in certain products and regions, necessitating careful consideration and adherence to regulatory guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 5335-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5335-24:
(6*5)+(5*3)+(4*3)+(3*5)+(2*2)+(1*4)=80
80 % 10 = 0
So 5335-24-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H8Cl2O/c13-9-6-10(12(15)11(14)7-9)8-4-2-1-3-5-8/h1-7,15H
5335-24-0Relevant academic research and scientific papers
Reaction of N-phenoxyphthalimide derivatives with aluminum chloride in benzene
Uto, Kensaku,Miyazawa, Etsuko,Ito, Katsuhiro,Sakamoto, Takeshi,Kikugawa, Yasuo
, p. 2593 - 2600 (2007/10/03)
N-Phenoxyphthalimides react with AlCl3 in benzene to form products of intramolecular N-C and inter molecular C-C bond formation via aryloxenium ion intermediates. N-Phenoxy derivatives having an electron-withdrawing substituent on the para position react with solvent benzene on the imide carbonyl, assisted by the neighboring oxygen atom, to produce N-(4-substituted phenoxy)-3,3-diphenyl-2,3-dihydroisoindol-1-ones.
