Interesting facts
Interesting Facts about 3,5-dibromo-2-hydroxy-benzaldehyde
3,5-dibromo-2-hydroxy-benzaldehyde is a fascinating compound that stands out due to its unique structure and properties. As a derivative of benzaldehyde, its complexity arises from the presence of two bromine atoms and a hydroxyl group on the benzene ring, which contributes to both its reactivity and potential applications. Here are some compelling points about this intriguing molecule:
- Medicinal Chemistry: Compounds like 3,5-dibromo-2-hydroxy-benzaldehyde play a significant role in the development of pharmaceuticals. The presence of the hydroxyl group can enhance solubility and bioactivity, making it a candidate for various biological evaluations.
- Antimicrobial Properties: Research has indicated that related compounds exhibit antimicrobial activity. This opens up avenues for exploration in developing new antiseptics or treatments for infections.
- Chemical Synthesis: The synthesis of this compound involves complex reaction mechanisms, which can serve as an excellent example for students studying reaction pathways in organic chemistry.
- Research Applications: It can be utilized in research settings to study the effects of bromination on the electronic properties of aromatic compounds, providing insight into how substituents influence reactivity.
- Colorimetric Properties: The incorporation of bromine atoms can also affect the colorimetric properties of the molecule, making it useful in applications such as dyes or indicators in various chemical reactions.
In summary, 3,5-dibromo-2-hydroxy-benzaldehyde serves as a rich subject for exploration in both educational and research contexts. Its multifaceted nature not only enhances our understanding of organic compounds but also holds promise for practical applications in different fields of science.
Synonyms
3,5-DIBROMOSALICYLALDEHYDE
90-59-5
3,5-Dibromo-2-hydroxybenzaldehyde
Dalyde
Benzaldehyde, 3,5-dibromo-2-hydroxy-
3,5-Dibromosalicylaldeyde
2-Hydroxy-3,5-dibromobenzaldehyde
MFCD00003318
Salicylaldehyde, 3,5-dibromo-
NSC 6221
EINECS 202-003-4
UNII-7A260PBI3A
BRN 1424739
7A260PBI3A
NSC-6221
DTXSID1021796
3-08-00-00188 (Beilstein Handbook Reference)
3,5-DIBROMOSALICYLALDEHYDE [MI]
4,6-Dibromo-2-formylphenol; Dalyde; NSC 6221
3,5-dibromsalicylaldehyd
Dembrexine Hydrochloride Monohydrate Imp. C (EP); Dembrexine Imp. C (EP); 3,5-Dibromo-2-hydroxybenzaldehyde; Dembrexine Hydrochloride Monohydrate Impurity C; Dembrexine Impurity C
Salicylaldehyde,5-dibromo-
3,5-dibromo-salicylaldehyde
CHEMBL229251
DTXCID601796
SCHEMBL2120180
NSC6221
3,5-Dibromo-2-hydroxybenzaldehyd
3,5-Dibromosalicylaldehyde, 98%
BDBM111000
Benzaldehyde,5-dibromo-2-hydroxy-
BCP06387
BBL023734
STK198699
AKOS000268598
FD29079
AC-15254
PD139179
SY036779
DB-022011
CS-0013288
D0188
NS00039365
EN300-18188
9P-929
F15422
Salicylaldehyde, 3,5-dibromo-(6CI,7CI,8CI)
SR-01000883702
SR-01000883702-1
US8614253, .3-31
Q27266799
Z57313905
F0910-0109
202-003-4
Solubility of 3,5-dibromo-2-hydroxy-benzaldehyde
The solubility of 3,5-dibromo-2-hydroxy-benzaldehyde can be influenced by several factors, including its molecular structure and interactions with solvents. This compound, with its unique functional groups, exhibits distinct solubility characteristics:
In summary, one can expect that 3,5-dibromo-2-hydroxy-benzaldehyde is more soluble in polar solvents due to its functional groups, but overall solubility may vary depending on the specific conditions and solvents used. As always, when working with chemical compounds, consulting solubility data specific to the laboratory environment is crucial for safety and effectiveness.