Interesting facts
Interesting Facts about 2,4,5-Tribromo-1H-Imidazole
2,4,5-Tribromo-1H-imidazole is a fascinating compound with a range of applications that showcase its importance in both scientific research and practical uses. Here are some key points to consider:
- Biological Activity: This compound has garnered attention for its potential biological applications, particularly as an antimicrobial and antifungal agent. Its bromine substitutions enhance its reactivity and effectiveness against various pathogens.
- Structural Features: The presence of bromine atoms in the imidazole ring plays a crucial role in altering the properties of the molecule, impacting its interactions with biological systems.
- Use in Research: 2,4,5-Tribromo-1H-imidazole is widely studied in medicinal chemistry for the development of new pharmaceuticals. Researchers are investigating its mechanisms of action and potential therapeutic applications.
- Environmental Impact: Its stability and persistent nature raise concerns regarding environmental bioaccumulation. Scientists are exploring the degradation pathways of this compound in various ecosystems.
- Comparative Chemistry: Compared to other halogenated imidazoles, 2,4,5-tribromo variants are unique in their ability to enhance biological activity, making them a subject of intense research.
This compound exemplifies the complex interplay between chemical structure and biological function. Its study not only enriches our understanding of imidazole derivatives but also illuminates potential pathways for disease treatment and environmental considerations. As we explore more about 2,4,5-tribromo-1H-imidazole, we delve into the broader implications of bromination in organic chemistry, showcasing how small modifications can lead to significant changes in function.
Synonyms
2,4,5-TRIBROMOIMIDAZOLE
2034-22-2
2,4,5-Tribromo-1H-imidazole
1H-Imidazole, 2,4,5-tribromo-
Imidazole, 2,4,5-tribromo-
EINECS 217-997-5
NSC 514965
BRN 0115314
AI3-62059
50V0252S9A
NSC-514965
DTXSID2022173
UNII-50V0252S9A
5-23-04-00465 (Beilstein Handbook Reference)
DTXCID702173
217-997-5
jcggpcddfxivqb-uhfffaoysa-n
MFCD00005184
Tribromoimidazole
2,5-Tribromoimidazole
Imidazole,4,5-tribromo-
2,4,5-tribromo imidazole
2,4,5-tribromo-imidazole
SCHEMBL69879
1H-Imidazole,4,5-tribromo-
CHEMBL363992
2,4,5-Tribromoimidazole, 97%
2,4,5-Tribromo-1H-imidazole #
CL2210
NSC514965
AKOS015835021
AC-7522
CS-W001961
AS-15002
NS00026589
T2266
EN300-140762
AC-907/25014002
Q27893870
Z1269217056
Solubility of 2,4,5-tribromo-1H-imidazole
The solubility of 2,4,5-tribromo-1H-imidazole is an intriguing aspect to explore, particularly due to its unique structure and the presence of multiple bromine atoms. This compound tends to exhibit varying solubility depending on the solvent used. Here are some key points to consider:
As a general rule, it’s essential to consider that the presence of bromine, a bulky and electronegative atom, significantly influences not only the solubility in various solvents but also the interaction with other chemical species. Thus, when working with 2,4,5-tribromo-1H-imidazole, one should always take into account these solubility characteristics, especially when designing experiments or synthesis pathways.