Thiosemicarbazone

ADVERTISEMENT

Identification

Molecular formula
C10H14BrN4OS
CAS Number
79-19-6
IUPAC Name
N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid
Molecular Weight
301.21g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4200g/cm3
Interesting facts

Interesting Facts about N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid

N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid is a fascinating compound that exhibits unique characteristics and applications, primarily in the fields of chemistry and pharmacology. Below are some interesting insights about this chemical entity:

  • Structural Complexity: The compound features a distinctive structure that includes both isothiazole and morpholine rings, contributing to its biological activity and potential therapeutic uses.
  • Isothiazole Influence: The presence of the isothiazole moiety, especially with a bromo and methyl substitution pattern, plays a crucial role in enhancing the compound's reactivity and biological interactions.
  • Biological Activity: Compounds with similar structures have shown promising results as antimicrobial agents, signaling a potential for this compound in treating infectious diseases.
  • Research Interest: The integration of thioic acid functionality suggests potential applications in developing pharmaceuticals, including inhibitors for specific biochemical pathways.
  • Synthesis Applications: This compound serves as an excellent focal point in synthetic organic chemistry, highlighting the importance of multi-step synthesis techniques and the role of functional group transformations.

In summary, N-[1-(4-bromo-3-methyl-isothiazol-5-yl)ethylidene]morpholine-4-carbohydrazonothioic acid is a noteworthy example of how structural diversity in chemical compounds can lead to novel applications in science. Its unique features inspire ongoing research and discovery.

ADVERTISEMENT