90221-61-7

Basic information

• Product Name: 2-bromo-3-hydroxy-4-methoxybenzoic acid
• Synonyms: 2-bromo-3-hydroxy-4-methoxybenzoic acid
• CAS NO: 90221-61-7
• Molecular Weight: 247.045
• Mol File: 90221-61-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-bromo-3-hydroxy-4-methoxybenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-3-hydroxy-4-methoxybenzoic acid(90221-61-7)
• EPA Substance Registry System: 2-bromo-3-hydroxy-4-methoxybenzoic acid(90221-61-7)

Safety Data

• Hazardous Substances Data: 90221-61-7(Hazardous Substances Data)

Upstream product

• 2973-58-2 2-bromoisovanillin 
• 859767-02-5 3-acetoxy-4-methoxy-benzonitrile 
• 51673-94-0 3-hydroxy-4-methoxy-benzaldehyde (E)-oxime 
• 850856-57-4 2-bromo-3-hydroxy-4-methoxy-benzonitrile 
• 52805-46-6 2-methoxy-5-cyanophenol 
• 621-59-0 isovanillin 

Downstream Products

• 108249-44-1 methyl 2-bromo-3-hydroxy-4-methoxybenzoate 

Relevant articles and documents

Design, Synthesis, and Biological Evaluation of Chalcone Derivatives as Novel Anticandidal Agents

Twenty chalcone derivatives were designed and synthesized with a view to developing novel anticandidal agents. All the compounds were evaluated for their antifungal activity against Candida albicans (ATCC 10231 and ten clinical isolates). Most of them exhibited moderate anticandidal potency with MIC values ranging from 2.0 to 32.0 μg/mL. Four compounds (T4, T6, T19, T20) displayed potent anticandidal activity with MIC values of 2.0 μg/mL. Compound T6 showed the most potent activity against Candida albicans (ATCC 10231 and four clinical isolates). In addition, attempts have also been made to correlate anticandidal activity to physicochemical properties. The results indicated that incorporation of halogen on the benzene ring is beneficial for anticandidal activity.