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(4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate

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Identification
Molecular formula
C12H22N4S3
CAS number
600-29-1
IUPAC name
(4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate
State
State

At room temperature, (4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate is in solid form.

Melting point (Celsius)
162.00
Melting point (Kelvin)
435.15
Boiling point (Celsius)
410.00
Boiling point (Kelvin)
683.15
General information
Molecular weight
308.48g/mol
Molar mass
308.4800g/mol
Density
1.2375g/cm3
Appearence

(4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate appears as a yellow to brown solid. The compound typically forms as a crystalline powder.

Comment on solubility

Solubility of (4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate

The solubility of (4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate can be quite complex, as it depends on various factors such as temperature, solvent type, and pH levels. Here are some key points to consider:

  • Polarity: The presence of both thioyl and dithioate groups suggests that this compound may have significant polar characteristics, which can influence its solubility in polar solvents like water.
  • Hydrophobic Interactions: The ethyl groups in the piperazine moiety can create hydrophobic interactions, possibly leading to reduced solubility in highly polar solvents.
  • Solvent Choice: Typically, compounds similar in structure to this one may exhibit better solubility in organic solvents such as methanol, ethanol, or dimethyl sulfoxide (DMSO).
  • Temperature Effects: Increased temperatures often enhance solubility; thus, heating the solvent may help dissolve the compound more effectively.
  • pH Sensitivity: If the substance is ionizable, variations in pH can also lead to changes in solubility, making it important to test under different conditions.

While detailed solubility data specific to this compound might be limited, understanding these factors can provide valuable insights. Keep in mind that solubility is not just a binary measure—it's a spectrum influenced by multiple external conditions that might warrant further investigation.

Interesting facts

Exploring (4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate

The compound known as (4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate presents a fascinating topic of study in the field of organic chemistry, particularly due to its unique structure and the potential applications in various scientific domains. Here are some intriguing facts that highlight its significance:

  • Unique Structure: This compound features a complex arrangement that includes piperazine rings and thiol groups, making it an interesting subject for studying the effects of various substituents on molecular properties.
  • Potential Biological Activities: Compounds like this one have been investigated for their biological activities, including antimicrobial, antitumor, and antiviral properties. Researchers are continuously exploring how structural modifications influence these activities.
  • Thiol Chemistry: The presence of thiol (-SH) groups allows for participation in various reactions, including redox reactions, which can be quite significant in medicinal chemistry.
  • Coordination Chemistry: This compound's ability to form coordination complexes with metal ions makes it relevant in coordination chemistry, providing opportunities for synthesizing novel materials with potential catalytic applications.
  • Industrial Applications: Sulfur-containing compounds, such as this one, often find applications in agrochemicals, pharmaceuticals, and materials science, further showcasing their versatility.

As one dives deeper into the chemistry of (4-ethylpiperazine-1-carbothioyl)sulfanyl 4-ethylpiperazine-1-carbodithioate, it becomes clear that understanding its properties can unlock pathways to advancing various fields, from medicinal chemistry to industrial applications. Its intricate structure not only contributes to its reactivity but also makes it a catalyst for creative thought in drug design and material development.

This compound truly exemplifies the interconnected nature of chemistry and other scientific disciplines!

Synonyms
BRN 0831511
DISULFIDE, BIS((4-ETHYL-1-PIPERAZINYL)THIOCARBONYL)
Bis((4-ethyl-1-piperazinyl)thiocarbonyl)disulfide
29053-34-7
DTXSID70183293
RefChem:339206
DTXCID80105784
SCHEMBL28396746