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

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Identification
Molecular formula
C18H34N4S4
CAS number
/goz1Pd656
IUPAC name
(4-isopropylpiperazine-1-carbothioyl)sulfanyl 4-isopropylpiperazine-1-carbodithioate
State
State

At room temperature, the compound is typically found in a solid state. The crystalline nature allows for its manipulation in various experimental settings without risk of loss through evaporation or liquid spillage. However, it should be handled with care to avoid any moisture absorption which could alter its properties.

Melting point (Celsius)
120.50
Melting point (Kelvin)
393.65
Boiling point (Celsius)
368.00
Boiling point (Kelvin)
641.15
General information
Molecular weight
388.65g/mol
Molar mass
388.6520g/mol
Density
1.1979g/cm3
Appearence
The compound is typically a crystalline solid that may vary in color from white to off-white. Underneath lighting suitable for detailed examination, it often displays a distinctive luster common with crystalline powders.
  • Crystalline structure is evident under magnification.
  • Potential for amorphous forms based on synthesis conditions.
Comment on solubility

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

The solubility of the compound (4-isopropylpiperazine-1-carbothioyl)sulfanyl 4-isopropylpiperazine-1-carbodithioate can be quite intriguing due to its complex structure. When considering solubility, several factors come into play:

  • Polarity: The presence of both thiol and thione functional groups suggests that the compound could exhibit varying degrees of polarity. As a result, its solubility can differ greatly in polar versus non-polar solvents.
  • Hydrogen Bonding: The possibility of forming hydrogen bonds can enhance the solubility in solvents capable of participating in hydrogen bonding, such as alcohols and water.
  • Solvent Compatibility: The compound is likely more soluble in organic solvents like chloroform or dimethyl sulfoxide (DMSO) while being less soluble, or even insoluble, in aqueous solutions due to the hydrophobic isopropyl groups.

In conclusion, while experimentation and empirical data are crucial for determining the exact solubility profile, one could summarize the solubility tendencies as:

  1. Potentially soluble in organic solvents.
  2. Limited solubility in water.
  3. Dependence on temperature and pH variations.

Therefore, to fully understand the solubility of (4-isopropylpiperazine-1-carbothioyl)sulfanyl 4-isopropylpiperazine-1-carbodithioate, one should explore multiple solvents and conditions, as solubility can be quite specific to the environment.

Interesting facts

Interesting Facts about (4-isopropylpiperazine-1-carbothioyl)sulfanyl 4-isopropylpiperazine-1-carbodithioate

(4-isopropylpiperazine-1-carbothioyl)sulfanyl 4-isopropylpiperazine-1-carbodithioate is an intriguing compound within the realm of organic chemistry. It exhibits features that highlight its potential applications and the unique characteristics of its structure.

Structure and Components

  • Thioester Derivative: This compound is a thioester, which is a functional group containing a sulfur atom bonded to a carbonyl. Thioesters play vital roles in biological processes, including energy transfer and enzyme activity.
  • Piperazine Framework: The presence of the piperazine ring imparts certain pharmacological properties, making this compound of interest in medicinal chemistry and drug design. Piperazines are known for their versatility and are commonly found in pharmaceutical agents.
  • Isopropyl Groups: The isopropyl substituents contribute to the hydrophobic character of the molecule, potentially affecting its biological activity and interactions.

Potential Applications

This compound opens doors to various fields, particularly:

  • Medicinal Chemistry: Due to its core structure, it may serve as a lead compound or scaffold for developing new therapeutic agents.
  • Nano-Materials: The unique properties of thiol and thioester functionality may allow for applications in the synthesis of nanoscale materials.
  • Agricultural Chemistry: It could also find relevance in creating novel pesticides or herbicides, leveraging its biochemical properties.

Scientific Exploration

Researchers are continually exploring compounds like this one to uncover:

  • Mechanistic pathways of action in biological systems.
  • Interactions with biomolecules, including proteins and nucleic acids.
  • Structural modifications that enhance its efficacy or reduce side effects in therapeutic applications.

In summary, (4-isopropylpiperazine-1-carbothioyl)sulfanyl 4-isopropylpiperazine-1-carbodithioate is not just another chemical; it embodies a junction of structural complexity and potential utility that intrigues scientists and chemistry students alike.

Synonyms
DISULFIDE, BIS((4-ISOPROPYL-1-PIPERAZINYL)THIOCARBONYL)
29053-35-8
RefChem:1083870
Bis((4-isopropyl-1-piperazinyl)thiocarbonyl)disulfide
BRN 0838961