Furosemide
- Molecular formula
- C12H11ClN2O5S
- CAS Number
- 54-31-9
- IUPAC Name
- 4-chloro-2-(2-furylmethylamino)-5-sulfamoyl-benzoic acid
- Molecular Weight
- 330.74g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6800g/cm3
- Synonyms
- furosemide
Identification
Interesting Facts about 4-Chloro-2-(2-furylmethylamino)-5-sulfamoyl-benzoic Acid
4-Chloro-2-(2-furylmethylamino)-5-sulfamoyl-benzoic acid is a fascinating compound with several noteworthy characteristics, particularly in the realm of medicinal chemistry.
Structural Features
- Sulfonamide Group: The presence of a sulfamoyl group imparts significant pharmacological properties, often associating this compound with antibacterial and diuretic properties.
- Chlorine Substituent: The chlorine atom enhances lipophilicity, which can affect the compound's ability to cross biological membranes.
- Aromatic Structure: The benzoic acid framework contributes to a variety of chemical reactivity, making it useful in synthesis and a target for structural modifications.
Applications
This compound belongs to a class of sulfonamide compounds, which have been historically significant in the development of antibiotics. They work primarily by:
- Inhibiting bacterial folic acid synthesis
- Exhibiting a broad-spectrum of activity against various pathogens
Biological Importance
4-Chloro-2-(2-furylmethylamino)-5-sulfamoyl-benzoic acid has shown promise in various fields. Some key points include:
- Potential Anticancer Activity: Compounds with similar structures have been researched for their effects in oncology.
- Research Interest: Ongoing studies aim to explore its mechanisms of action and enhance its therapeutic efficacy.
Quote from the Pharmacological Field
As one researcher put it, “The sulfonamide class continues to be a cornerstone in the development of newer therapeutic agents.” This statement underscores the ongoing relevance of compounds like 4-chloro-2-(2-furylmethylamino)-5-sulfamoyl-benzoic acid in the pharmaceutical landscape.
In summary, the multifaceted nature of 4-Chloro-2-(2-furylmethylamino)-5-sulfamoyl-benzoic acid makes it a compound of great interest, bridging the gap between synthetic chemistry and practical medical applications.