Interesting facts
Interesting Facts About 3,5-Dibromo-N-(4-Bromophenyl)-2-Hydroxy-Benzamide
This compound, known as 3,5-dibromo-N-(4-bromophenyl)-2-hydroxy-benzamide, is a fascinating member of the larger class of organic compounds known as brominated aromatic compounds. Its unique structural features provide numerous avenues for research and application.
Chemical Structure and Properties
- Bromination: The presence of multiple bromine atoms enhances the compound's reactivity and introduces significant polar characteristics, which can affect its interactions in biological systems.
- Hydroxy Group: The hydroxy group (-OH) contributes to hydrogen bonding potential, which can enhance solubility and stability in specific solvents.
- Aromatic Nature: Its aromatic rings provide a platform for electronic delocalization, which can influence properties like UV-Vis absorption and reactivity toward electrophiles.
Potential Applications
The unique features of this compound position it as a suitable candidate for various applications:
- Pharmaceutical Research: Compounds like these often serve as vital components in drug design, particularly in targeting specific biological pathways.
- Material Science: Due to their bromination, these compounds may find utility in developing flame retardants and other specialized materials.
- Analytical Chemistry: Its distinct properties make it a candidate for use as a marker or standard in spectroscopic analyses.
Noteworthy Insights
As a student or scientist exploring this compound, you might find it intriguing to think about:
- Reaction Mechanisms: Consider how the bromine atoms can influence nucleophilic substitution reactions.
- Pharmacokinetics: Research how the structural components might affect absorption, distribution, metabolism, and excretion in biological systems.
- Environmental Impact: Investigate potential environmental effects stemming from the compound’s stability and persistence in ecological settings.
In summary, 3,5-dibromo-N-(4-bromophenyl)-2-hydroxy-benzamide represents a rich field of study due to its complex structure and multifaceted applications. Future research can uncover even more about this fascinating compound and its potential uses in chemistry and beyond.
Synonyms
Tribromsalan
87-10-5
Agramed
3,5-Dibromo-N-(4-bromophenyl)-2-hydroxybenzamide
TRIBROMOSALICYLANILIDE
3,4',5-Tribromosalicylanilide
Temasept IV
Tribromsalanum
Trisanil
Trisanyl
Tempasept II
Temasept II
Sherstat TBS
Vancide TBS
Tuasol 100
Tribromosalicyanilide
ET-394
Stecker asc-4
TBS 95
NSC-20526
Caswell No. 863
ASC-4
3,5-Dibromosalicylic acid p-bromoanilide
Tribromsalanum [INN-Latin]
CCRIS 5745
Tribromsalan [USAN:INN:BAN]
CHEBI:127105
WR 34912
6MCE3VTF0O
Salicylanilide, 3,4',5-tribromo-
EINECS 201-723-6
ENT 25516
EPA Pesticide Chemical Code 077404
BRN 2146888
BENZAMIDE, 3,5-DIBROMO-N-(4-BROMOPHENYL)-2-HYDROXY-
DTXSID4026181
3,5-Dibromo-N-(4-bromo-phenyl)-2-hydroxy-benzamide
AI3-25516
Tuasol 100 (TN)
TRIBROMSALAN [MI]
TRIBROMSALAN [INN]
TRIBROMSALAN [USAN]
TRIBROMSALAN [MART.]
WR-34912
TRIBROMSALAN [WHO-DD]
DTXCID606181
NSC20526
1322-38-9
Diaphene
Tribromsalanum (INN-Latin)
TRIBROMSALAN (MART.)
Temacept
DTXSID101060806
201-723-6
3,5,4'-Tribromosalicylanilide
Tribromosalan
TBS
Tribromsalen
Tuasol
Tuasal 100
NCGC00159476-02
CAS-87-10-5
Salicylanilide, tribromo-
UNII-6MCE3VTF0O
tribomsalan
Tuasal
Tribromosalicylanilide, 3,4',5-
MFCD00045740
Hilomid (Salt/Mix)
Diaphene (Salt/Mix)
Lamar L-300
Tribromsalan (USAN/INN)
3,5-Tribromosalicylanilide
Epitope ID:114087
Oprea1_401911
MLS004773969
3,4',5-Tribromosalicylanide
CHEMBL24944
SCHEMBL121315
Salicylanilide,4',5-tribromo-
WLN: QR BE DE FVMR DE
3,5,4''-Tribromosalicylanilide
KVSKGMLNBAPGKH-UHFFFAOYSA-
BDBM234329
Tox21_111700
Tox21_202442
Tox21_303223
NSC 20526
STK301503
AKOS003291727
Tox21_111700_1
NCGC00159476-03
NCGC00159476-04
NCGC00159476-05
NCGC00159476-06
NCGC00159476-09
NCGC00257186-01
NCGC00259991-01
SMR001551623
NS00004403
T0356
D06218
D92329
SBI-0653852.0001
Benzamide,5-dibromo-N-(4-bromophenyl)-2-hydroxy-
3,5-dibromo-N-(4-bromophenyl)-2-hydroxy-benzamide
BRD-K09118247-001-03-3
Q27219423
3,5-Dibromo-N-(4-bromophenyl)-2-hydroxybenzamide (31)
InChI=1/C13H8Br3NO2/c14-7-1-3-9(4-2-7)17-13(19)10-5-8(15)6-11(16)12(10)18/h1-6,18H,(H,17,19)
Solubility of 3,5-dibromo-N-(4-bromophenyl)-2-hydroxy-benzamide
The compound 3,5-dibromo-N-(4-bromophenyl)-2-hydroxy-benzamide exhibits specific solubility characteristics that can be summarized as follows:
Furthermore, it is noteworthy that functional groups, such as the hydroxyl group, tend to enhance solubility in water compared to pure hydrocarbons or halogenated compounds, making it partially soluble. In conclusion, the solubility of 3,5-dibromo-N-(4-bromophenyl)-2-hydroxy-benzamide is influenced by its structural components and the nature of the solvent utilized.