Furosemide

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Identification

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
Interesting facts

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.

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