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Chlormercuric chloride

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Identification
Molecular formula
C10H4Cl6HgNO2
CAS number
58-89-9
IUPAC name
ethyl-(1,7,8,9,10,10-hexachloro-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-yl)mercury
State
State

At room temperature, the compound appears as a solid. Specific details of appearance can vary, but generally characterized by stability under standard conditions among terminated end groups of similar mercury-based compounds.

Melting point (Celsius)
244.00
Melting point (Kelvin)
517.15
Boiling point (Celsius)
252.00
Boiling point (Kelvin)
525.15
General information
Molecular weight
515.49g/mol
Molar mass
515.4920g/mol
Density
2.9010g/cm3
Appearence

Ethyl-(1,7,8,9,10,10-hexachloro-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-yl)mercury, typically known in simpler forms as a chlormercuric compound, can be characterized by looking at similar compounds which are generally colorless or white crystalline solids. The exact appearance needs clear referencing from the precise compound definition and sources.

Comment on solubility

Solubility of Ethyl-(1,7,8,9,10,10-hexachloro-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-yl)mercury

The solubility of the compound ethyl-(1,7,8,9,10,10-hexachloro-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-yl)mercury is influenced by several factors, including its unique structural characteristics and the presence of functional groups. Due to its complex molecular architecture, this compound exhibits specific solubility properties in various solvents.

Factors Affecting Solubility:

  • Polarity: The presence of electronegative chlorine atoms increases the polarity of the molecule, suggesting that it may have limited solubility in nonpolar solvents.
  • Mercury Content: The inclusion of mercury in the structure often leads to increased hydrophobic characteristics, impacting solubility in aqueous environments.
  • Hydrogen Bonding: Functional groups capable of hydrogen bonding can enhance solubility in polar solvents, although the complex structure may hinder such interactions.

In general, high chlorination tends to decrease the solubility of organic compounds in water, while promoting solubility in organic solvents.

Practical Implications:

Due to its expected characteristics, ethyl-(1,7,8,9,10,10-hexachloro-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-yl)mercury may be more soluble in:

  • Organic solvents such as dichloromethane or acetone
  • Less soluble in water due to hydrophobic attributes

Understanding the solubility of this compound is crucial for practical applications, as it affects its bioavailability, environmental impact, and potential uses in chemical processes. Further empirical investigations would be beneficial to elucidate the precise solubility characteristics of this intriguing compound.

Interesting facts

Interesting Facts about Ethyl-(1,7,8,9,10,10-hexachloro-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-yl)mercury

This remarkable compound belongs to a class of organomercury compounds, which are known for their significant applications in various fields, particularly in the realm of chemistry and biochemistry.

Key Features

  • Versatile Applications: Organomercury compounds have historically been used as fungicides and antibacterial agents, especially in agriculture.
  • Complex Structure: The intricate structure of this compound showcases the diverse bonding patterns in organic chemistry, making it a subject of interest for synthetic chemists.
  • Environmental Impact: Mercury compounds have garnered attention for their potential ecological risks, emphasizing the need for careful handling and study.
  • Medicinal Chemistry: Research into organomercury compounds might lead to new therapeutic developments, notably in targeting specific biological pathways.

Cultural and Historical Relevance

Historically, mercury compounds were widely utilized in medicine, although their toxic nature has led to a decline in use due to health risks.

As noted by many scientists, “The balance between utilizing compounds for beneficial properties while mitigating their toxic effects is crucial in modern chemistry.” This highlights the ongoing evolution of how we approach chemical safety and application.

Research Opportunities

The synthesis and study of this compound open new avenues for research, particularly in:

  1. Understanding molecular interactions in biological systems.
  2. Developing safer alternatives to hazardous chemicals.
  3. Investigating methods to remediate mercury contamination in environments.

In conclusion, ethyl-(1,7,8,9,10,10-hexachloro-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-yl)mercury serves not only as a subject of scientific inquiry but also as a reminder of the intricate balance between chemistry’s contributions to society and the responsibility that comes with them.

Synonyms
2597-93-5
Ethyl(4,5,6,7,8,8-hexachloro-3a,4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dionato-kappaN2)mercury
Ethylmercurichlorendimide
50-CS-46
DTXSID7044558
Mercury, ethyl(4,5,6,7,8,8-hexachloro-1,3,3a,4,7,7a-hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl)-
ethyl-(1,7,8,9,10,10-hexachloro-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-yl)mercury
Mercury, ethyl(4,5,6,7,8,8-hexachloro-3a,4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dionato-.kappa.N2)-
Ethylmercury(1+);1,7,8,9,10,10-hexachloro-5-oxo-4-azatricyclo[5.2.1.02,6]deca-3,8-dien-3-olate
SCHEMBL5933970
DTXCID5024558
NSC22200
Tox21_303854
AKOS024429069
NCGC00357007-01
CAS-2597-93-5
NS00122068
5-Norbornene-2, 1,4,5,6,7,7-hexachloro-N-(ethylmercuri)-
WLN: T C555 A DVNV IUTJ AG AG BG E-HG-2 HG IG JG
Mercury,4,5,6,7,7-hexachloro-5-norbornene-2,3-dicarboximidato)-
Mercury, ethyl(1,4,5,6,7,7-hexachloro-5-norbornene-2,3,-dicarboximido)
4,3(2H)-dione, 4,5,6,7,8,8-hexachloro-2-(ethylmercurio)-3a,4,7,7a-tetrahydro-
4,6,7,7-Hexachloro-N-(ethylmercuri)-1,2,3,6-tetrahydro-3,6-endomethanophthalimide
N-(Ethylmercuri)-1,3,6-tetrahydro-3,6-endomethano-3,4,5,6,7,7-hexachlorophthalimide
N-(Ethylmercuri)-1,4,6,6,7,7-hexa-cl-bicyclo(2.2.1)hept-5-ene-2,3-dicarboximide
N-(Ethylmercuri)-1,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboximide
N-(Ethylmercuri)-3,4,5,6,7,7-hexachloro-3,6-endomethylene-1,2,3,6-tetrahydrophthalimide
N-(Ethylmercuri)-3,5,6,7,7-hexachloro-3,6-endomethylene-1,2,3,6-tetrahydrophthalimide
N-ethylmercuri-1,2,3,6tetrahydro-3,6-endomethano-3,4,5,6,7,7-hexachlorophthalimide
4,7-Methano-1H-isoindole-1,3(2H)-dione, 4,5,6,7,8,8-hexachloro-2-(ethylmercurio)-3a,4,7,7a-tetrahydro-
Mercury,5,6,7,8,8-hexachloro-1,3,3a,4,7,7a-hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl)-