Interesting facts
Exploring 5-Bromoindoline-2,3-dione
5-Bromoindoline-2,3-dione is a fascinating compound that has garnered attention in the realms of organic chemistry and medicinal research. Here are some intriguing facts about this compound:
- Structural Significance: This compound features a unique indoline core which is pivotal in many biological activities. Its structure includes a bromine atom, which can significantly enhance the compound's reactivity and potential applications in synthesis.
- Potential Biological Activities: 5-Bromoindoline-2,3-dione and its derivatives have been studied for their antimicrobial and antitumor properties. Researchers are particularly interested in how the introduction of bromine might influence its pharmacological profile.
- Synthetic Utility: The compound serves as a building block in organic synthesis, showcasing its importance in the development of various molecules. Its reactivity allows for the introduction of diverse functional groups, making it a pivotal compound in the design of more complex chemical entities.
- Research Applications: The investigation of this compound contributes to the broader field of medicinal chemistry, where understanding structure-activity relationships is key. Its derivatives may offer insights into new therapeutic avenues for treating a range of diseases.
- Advancements in Materials Science: Beyond its biological applications, this compound has potential uses in materials science, especially in the creation of organic semiconductors due to its planar structure and ability to form π-stacks.
In summary, 5-Bromoindoline-2,3-dione is much more than just a chemical entity. Its diverse potential applications across various fields make it a subject of continued interest for both chemists and researchers alike.
Synonyms
5-Bromoisatin
87-48-9
5-Bromoindoline-2,3-dione
5-Bromo-1H-indole-2,3-dione
5-Bromoindole-2,3-dione
Isatin, 5-bromo-
5-Bromisatin
1H-Indole-2,3-dione, 5-bromo-
5-Bromisatin [Czech]
Bromoisatin
NSC 4980
5-bromo-2,3-dihydro-1H-indole-2,3-dione
EINECS 201-747-7
INDOLE-2,3-DIONE, 5-BROMO-
BRN 0383760
5-bromo-2-hydroxy-3H-indol-3-one
DTXSID30236037
5-21-10-00264 (Beilstein Handbook Reference)
NSC-4980
5-bromo isatin
5-bromo-isatin
MFCD00005719
Indole-2, 5-bromo-
Isatin-based compound, 34
1H-Indole-2, 5-bromo-
5-Bromo-2,3-indolinedione
DZU75P8VY8
WLN: T56 BMVVJ GE
SCHEMBL136581
5-bromo-1H-indole-2,3dione
CHEMBL115897
BDBM22814
DTXCID30158528
NSC4980
CHEBI:149786
5-Bromo -1H-indole-2,3-dione
5-Bromo-1H-indole-2,3-dione #
BCP04280
STR04158
MFCD00149345
STK364356
STL140691
5-Bromoisatin, technical grade, 90%
AKOS000200674
AKOS002375882
CS-W007383
FB19242
FS-2520
SB66105
1H-Indole-2,3-dione, 5-bromo-(9CI)
AC-14581
DB-026328
B1566
NS00039198
EN300-18123
F11278
SR-01000402436
SR-01000402436-1
Z57833927
F0900-5717
5-Bromo-indole-2,3-dione;5-Bromo-isatin;5-Bromo-1H-indole-2,3-dione
201-747-7
Solubility Characteristics of 5-bromoindoline-2,3-dione
5-bromoindoline-2,3-dione, a compound notable for its unique chemical structure, exhibits specific solubility properties. Understanding its solubility can provide valuable insights for applications in various fields. Here’s what we know:
In summary, while 5-bromoindoline-2,3-dione is generally soluble in polar solvents and shows increased solubility with rising temperatures, its solubility in non-polar systems remains limited. Understanding these properties can be crucial for its application in scientific research and industry.