50638-08-9 Usage
Uses
Used in Pharmaceutical Industry:
5-BROMO-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID is used as a building block for the synthesis of various drug molecules, contributing to the development of new pharmaceuticals with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 5-BROMO-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID is used as a reagent, particularly for the preparation of heterocyclic compounds, which are important in the creation of complex organic molecules and pharmaceuticals.
Used in Research and Development:
5-BROMO-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID is utilized as a research tool for studying benzofuran-based compounds and their biological effects, aiding in the advancement of scientific knowledge and the discovery of new therapeutic agents.
Used in Anti-Cancer Applications:
5-BROMO-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID is being studied for its potential anti-cancer properties, with the aim of developing new treatments for various types of cancer.
Used in Anti-Inflammatory Applications:
5-BROMO-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID is also being investigated for its anti-inflammatory properties, which could lead to the development of new medications for the treatment of inflammatory conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 50638-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,3 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50638-08:
(7*5)+(6*0)+(5*6)+(4*3)+(3*8)+(2*0)+(1*8)=109
109 % 10 = 9
So 50638-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H7BrO3/c1-5-7-4-6(11)2-3-8(7)14-9(5)10(12)13/h2-4H,1H3,(H,12,13)/p-1
50638-08-9Relevant academic research and scientific papers
Convenient synthesis of some 3-phenyl-1-benzofuran-2-carboxylic acid derivatives as new potential inhibitors of ClC-Kb channels
Piemontese, Luca,Carbonara, Giuseppe,Fracchiolla, Giuseppe,Laghezza, Antonio,Tortorella, Paolo,Loiodice, Fulvio
, p. 2865 - 2872 (2011/04/24)
Improved experimental conditions were carried out for the preparation in high yields of some 3-phenyl-1-benzofuran-2-carboxylic acids, potent inhibitors of ClC-K chloride channels. A one-pot condensation-cyclization was set up starting from different 2-hy
Biaryl sulfonamides and methods for using same
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Page/Page column 41, (2010/02/12)
The present invention relates to biaryl sulfonamides and their use as, for example, metalloproteinase inhibitors.
