Thiosemicarbazone
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- 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
Identification
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.