Interesting facts
Interesting Facts about (4-Carboxyphenyl)mercury Hydrate
(4-Carboxyphenyl)mercury hydrate is a fascinating organomercurial compound with notable properties and applications in various fields, particularly in chemistry and environmental science. Here are some key points to understand its significance:
- Organomercurial Compound: This compound belongs to a class of organomercurials, which are organic compounds that contain mercury. Organomercurials are of great interest due to their implications in biological systems and their roles in environmental toxicity.
- Application in Organic Synthesis: (4-Carboxyphenyl)mercury hydrate is often employed in organic synthesis as a reagent. It can facilitate the formation of C-C bonds, making it valuable in the construction of complex molecular architectures.
- Environmental Concerns: Mercury compounds, including this one, have raised significant environmental concerns due to their toxicity and potential for bioaccumulation. Studies often focus on minimizing environmental impact and understanding their long-term effects on ecosystems.
- Biological Activity: Research indicates that compounds like (4-carboxyphenyl)mercury can interact with biomolecules, leading to alterations in cellular processes. This property has made it a subject of interest in pharmaceutical research, particularly in understanding how mercury influences biological systems.
- Quotes from Research: One notable research article stated, “The study of organomercurials such as (4-carboxyphenyl)mercury is crucial for developing safe practices in pharmacology and environmental chemistry.” Such insights underline the importance of understanding these compounds.
In conclusion, (4-Carboxyphenyl)mercury hydrate stands as a compelling subject within the realm of chemistry, bridging areas of organic synthesis and environmental safety. Its unique properties and implications for both human health and ecological systems make it a critical focus for ongoing scientific inquiry.
Synonyms
p-hydroxymercuribenzoic acid
(p-carboxyphenyl)hydroxymercury
1126-48-3
mercury, (p-carboxyphenyl)hydroxy-
(4-carboxyphenyl)mercury;hydrate
(4-carboxyphenyl)(hydroxy)mercury
(4-carboxylatophenyl)hydroxymercurate(1-) hydrogen
Mercurate(1-), (4-carboxylatophenyl)hydroxy-, hydrogen
848QN6RR3O
CHEBI:49644
DTXSID601319329
DTXCID20208965
Mercurate(1-), (4-carboxylatophenyl)hydroxy-, hydrogen (9CI)
hydroxymercuribenzoic acid, p-
4-(HYDROXYMERCURY)BENZOIC ACID
UNII-848QN6RR3O
Mercury, sodium salt
Mercury, monosodium salt
Mercurate(1-), sodium
CHEMBL78771
SCHEMBL678164
NSC1048
BDBM50351172
DB01671
P-HYDROXYMERCURIBENZOIC ACID, SODIUM SALT
Solubility of (4-carboxyphenyl)mercury Hydrate
(4-carboxyphenyl)mercury, often encountered in its hydrate form, exhibits interesting solubility characteristics. Its behavior in various solvents can be influenced by several factors due to its unique structure. Here are some key points to consider:
In summary, the solubility of (4-carboxyphenyl)mercury hydrate is a multifaceted phenomenon influenced by solvent polarity, temperature, and solution pH. As such, understanding these factors can be crucial for applications in chemical processes and formulations.