5468-74-6 Usage
Description
2-(2-bromobenzyl)-4-methylphenol, also known as 2-bromo-4-methyl-6-phenylphenol, is an organic compound characterized by the chemical formula C14H13BrO. It is a phenolic compound distinguished by the presence of a bromine atom and a benzyl group attached to a phenol ring. This chemical is recognized for its potent antimicrobial properties, which make it a valuable component in various applications.
Uses
Used in Antimicrobial Applications:
2-(2-bromobenzyl)-4-methylphenol is utilized as an antiseptic and disinfectant in various commercial products such as soaps, lotions, and creams. Its strong antimicrobial properties contribute to the prevention of bacterial and fungal infections, making it a common ingredient in personal care and hygiene products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-(2-bromobenzyl)-4-methylphenol is studied for its potential in treating bacterial and fungal infections. Its antimicrobial action is being explored for the development of new therapeutic agents to combat resistant strains of pathogens.
Used in Environmental Sanitation:
2-(2-bromobenzyl)-4-methylphenol is also considered for use in environmental sanitation to control microbial growth in various settings, such as in water treatment and surface disinfection, due to its broad-spectrum antimicrobial activity.
However, it is important to note that the use and production of 2-(2-bromobenzyl)-4-methylphenol are regulated due to concerns about its potential environmental and health effects. This regulation ensures that its benefits are realized while minimizing any adverse impacts.
Check Digit Verification of cas no
The CAS Registry Mumber 5468-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5468-74:
(6*5)+(5*4)+(4*6)+(3*8)+(2*7)+(1*4)=116
116 % 10 = 6
So 5468-74-6 is a valid CAS Registry Number.
5468-74-6Relevant articles and documents
Intramolecular 9-membered hydrogen bonding of 2-arylmethylphenols having carbonyl groups at 2′-position
Yoshimi, Yasuharu,Maeda, Hajime,Hatanaka, Minoru,Mizuno, Kazuhiko
, p. 9425 - 9431 (2007/10/03)
Thermodynamic parameters of nine-membered intramolecular hydrogen bonding between carbonyl groups and phenolic hydroxyl groups of 2-arylmethylphenols having methoxycarbonyl, dimethylcarbamoyl, and formyl groups were determined by variable temperature 1H NMR studies and van't Hoff analysis. The enthalpy of the hydrogen bonding was related to the electron-withdrawing ability of the substituents on the phenol and the basicity of the carbonyl group. The entropy loss of the hydrogen bonding was dependent on the rotation freedom of the phenol group. The enthalpy of nine-membered intramolecular hydrogen bonding between carbonyl groups and phenolic hydroxyl groups of 2-arylmethylphenols was related to the electron-withdrawing ability of the substituents on the phenol and the basicity of the carbonyl group. The entropy loss was dependent on the rotation freedom of the phenol group.