62547-35-7

Usage

Uses

Used in Pharmaceutical Industry:
PHENYL 3,5-DIBROMO-2-HYDROXYBENZOATE is used as a drug candidate for its anti-inflammatory and antimicrobial activities, making it a promising compound for the development of new medications.
Used in Cosmetic Industry:
PHENYL 3,5-DIBROMO-2-HYDROXYBENZOATE is used as an antioxidant and UV-absorbing agent in cosmetic products, providing protection against harmful UV radiation and oxidative stress, thus contributing to the maintenance of skin health and appearance.
Overall, PHENYL 3,5-DIBROMO-2-HYDROXYBENZOATE is a versatile compound with various applications in different fields, including pharmaceutical and cosmetic industries, due to its unique properties and potential benefits.

InChI:InChI=1/C13H8Br2O3/c14-8-6-10(12(16)11(15)7-8)13(17)18-9-4-2-1-3-5-9/h1-7,16H

Upstream product

• 118-55-8 phenyl Salicylate 
• 64-19-7 acetic acid 
• 3147-55-5 3,5-dibromosalicylic acid 
• 108-95-2 phenol 
• 64-17-5 ethanol 
• 7726-95-6 bromine 

Downstream Products

• 3147-55-5 3,5-dibromosalicylic acid 
• 20907-64-6 C₁₃H₁₀Br₂N₂O₂ 
• 1334311-48-6 C₁₃H₁₀Br₂N₂O₂ 

Relevant academic research and scientific papers

A new group of potential antituberculotics: N-(2-pyridylmethyl) salicylamides and N-(3-pyridylmethyl)salicylamides

As a part of our systematic study of antimycobacterially active derivatives of salicylamides, a series of nineteen derivatives of N-(2-pyridylmethyl) salicylamides and N-(3-pyridylmethyl)salicylamides was synthesised. The compounds exhibited in vitro activity against Mycobacterium tuberculosis and M. avium. Their lipophilicity, RM, was measured by thin layer chromatography on silica gel impregnated with trioctadecylsilane and the logarithm of the partition coefficient (octanol-water), logP, was calculated. Both the parameters of lipophilicity correlated. The quantitative relationship between the structure and antimycobacterial activity was calculated. Antimycobacterial activity increased with an increase in lipophilicity. The N-(2-pyridylmethyl)salicylamide derivatives were more active than the derivatives of isomeric N-(3-pyridylmethyl)salicylamides. The geometry of compounds was calculated and the calculation was verified by measuring the length of the hydrogen bond between hydroxyl and carbonyl groups on the salicylic moiety.