Interesting facts
Interesting Facts about 3-Chloro-4-Hydroxy-5-Methoxy-Benzaldehyde
3-Chloro-4-hydroxy-5-methoxy-benzaldehyde, a unique aromatic compound, arouses curiosity due to its fascinating structural features and potential applications. Here are some captivating aspects to consider:
- Structure and Properties: This compound is characterized by the presence of both a chloro group and a methoxy group, which significantly influence its reactivity and interaction with other substances.
- Bioactivity: Compounds similar to 3-chloro-4-hydroxy-5-methoxy-benzaldehyde have been studied for their biological activities. Some derivatives have shown promise in anti-inflammatory and antioxidant properties, which underscores the potential relevance of this compound in medicinal chemistry.
- Synthetic Applications: This compound can serve as an important building block in organic synthesis, offering a pathway to more complex molecules. The presence of multiple functional groups facilitates various chemical reactions, potentially leading to the creation of novel compounds.
- Chemical Symbolism: The structure of this compound, incorporating the aldehyde functional group, makes it an excellent candidate for further functionalization, adding to its versatility in chemical synthesis.
- Cultural Relevance: Compounds featuring similar functional groups are often explored for their application in flavoring and fragrance industries, as well as in the development of agrochemicals and pharmaceuticals.
As a scientist or student delving into the realm of organic chemistry, understanding such complex compounds not only enriches our knowledge but also opens avenues for innovative research and development. Every molecule, like 3-chloro-4-hydroxy-5-methoxy-benzaldehyde, holds the potential to unlock new scientific wonders.
Synonyms
3-CHLORO-4-HYDROXY-5-METHOXYBENZALDEHYDE
19463-48-0
5-Chlorovanillin
Vanillin, 5-chloro-
3-Chlorovanillin
6L2HJ5NXQ8
NSC-45929
243-086-7
RefChem:500551
Benzaldehyde, 3-chloro-4-hydroxy-5-methoxy-
MFCD00016982
3-Chloro-4-hydroxy-5-methoxy-benzaldehyde
3-chloro-4-hydroxy-5-methoxy benzaldehyde
61670-76-6
5-chlorovanilline
5-chloro vanillin
EINECS 243-086-7
NSC 45929
CHLORO-4-HYDROXY-3-METHOXYBENZALDEHYDE
UNII-6L2HJ5NXQ8
SCHEMBL564090
CHEMBL2205139
DTXSID9075161
ALBB-026361
CS-M0909
NSC45929
BBL023134
SBB001593
STK033666
AKOS000111549
FC70138
FS-5847
SY018867
DB-044866
ST4045691
3-Chloro-4-hydroxy-5-methoxybenzaldehyde #
NS00026344
EN300-07241
W18340
Z56948379
3-Chloro-4-hydroxy-5-methoxybenzaldehyde;3-Chlorovanillin
Solubility of 3-chloro-4-hydroxy-5-methoxy-benzaldehyde
3-chloro-4-hydroxy-5-methoxy-benzaldehyde, a compound that features a benzene ring with multiple functional groups, exhibits intriguing solubility characteristics. Its solubility is influenced by the presence of polar -OH (hydroxyl) and -OCH3 (methoxy) groups, which tend to enhance interaction with polar solvents.
Solubility Characteristics:
As a general rule, compounds with greater hydrophilic character (like those with hydroxyl and methoxy groups) tend to be more soluble in water, while their hydrophobic counterparts, particularly those lacking polar functional groups, prefer organic solvents. This interplay results in the compound being a versatile participant in various chemical reactions and formulations.
In summary, the solubility of 3-chloro-4-hydroxy-5-methoxy-benzaldehyde is enhanced in polar environments, highlighting the paramount role of its functional groups in defining its chemical behavior.