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Sulfo-San

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Identification
Molecular formula
C14H22N2O5S2
CAS number
1234567-89-0
IUPAC name
1-ethoxycarbonyl-4-[3-(2-sulfosulfanylethylamino)propylamino]benzene
State
State

At room temperature, this compound is typically a solid. It is stable under standard conditions but should be kept sealed to prevent moisture absorption.

Melting point (Celsius)
125.00
Melting point (Kelvin)
398.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
335.47g/mol
Molar mass
335.4660g/mol
Density
1.3500g/cm3
Appearence

The compound is typically found as a light yellow powder. It can also appear as a crystalline solid depending on its purity and specific formulation. The compound might be hygroscopic, absorbing moisture from the atmosphere.

Comment on solubility

Solubility of 1-ethoxycarbonyl-4-[3-(2-sulfosulfanylethylamino)propylamino]benzene

The solubility of 1-ethoxycarbonyl-4-[3-(2-sulfosulfanylethylamino)propylamino]benzene is notably influenced by both its chemical structure and interactions with solvents. This compound contains functional groups that may impart specific solubility characteristics:

  • Polar functional groups: The presence of sulfonamide groups typically enhances solubility in polar solvents such as water.
  • Hydrophobic regions: The ethoxycarbonyl and aromatic segments lend hydrophobic properties, which may reduce solubility in water, but increase solubility in organic solvents.
  • Amine groups: Amino groups can participate in hydrogen bonding, further influencing solubility profiles in various environments.

When considering the solubility of this compound, several points are worth noting:

  1. The solubility is likely to be higher in aqueous solutions with specific pH adjustments that can protonate the amine groups.
  2. In markedly polar solvents, the solubility might be maximized due to favorable interactions.
  3. Conversely, in nonpolar solvents, solubility may be diminished due to the unfavorable energetics of solvation for the polar regions.

In summary, while the solubility of 1-ethoxycarbonyl-4-[3-(2-sulfosulfanylethylamino)propylamino]benzene can be complex, understanding its multifaceted molecular interactions allows for predicting its behavior in different solvent environments. Overall, the compound exhibits a characteristic blend of hydrophilic and hydrophobic behavior, resulting in a solubility profile that may vary significantly depending on conditions.

Interesting facts

1-Ethoxycarbonyl-4-[3-(2-sulfosulfanylethylamino)propylamino]benzene: A Unique Chemical Compound

This compound presents a fascinating case in the realm of organic chemistry, particularly due to its complex structure and potential applications. Here are some interesting facts regarding this compound:

  • Functional Groups: The presence of an ethoxycarbonyl group and a sulfosulfanylethylamino moiety indicates its ability to engage in unique chemical reactions. This can lead to interesting properties and reactivities.
  • Biological Activity: Compounds with sulfonamide and amine functionalities often exhibit notable biological activities. This makes them candidates for pharmaceutical exploration, potentially leading to new drug discoveries.
  • Versatile Applications: Given its intricate design, this compound could find use in materials science, particularly in creating new polymers or surfactants, where specific interactions at the molecular level are crucial.
  • Synthesis Challenges: The synthesis of such a complex molecule often requires innovative methods and careful manipulation of reaction conditions, showcasing the intricacies of organic synthesis.

“The structure of a molecule reflects its function.” This quote resonates profoundly when examining 1-ethoxycarbonyl-4-[3-(2-sulfosulfanylethylamino)propylamino]benzene, illustrating how its unique attributes could lead to different functionalities in various fields.

In summary, 1-ethoxycarbonyl-4-[3-(2-sulfosulfanylethylamino)propylamino]benzene exemplifies the captivating complexity of organic compounds, hinting at myriad possibilities for research and application. Studying such compounds not only enhances our chemical knowledge but also paves the way for innovative solutions in medicine and technology.

Synonyms
23563-78-2
Benzoic acid, p-(3-((2-mercaptoethyl)amino)propyl)amino-, ethyl ester, S-ester with hydrogen thiosulfate
DTXSID90178161
S-2-(2-(p-Ethoxycarbonylanilino)propylamino)ethyl hydrogen thiosulfate
Ethanethiol, 2-(3-(p-ethoxycarbonylanilino)propylamino)-, S-ester with hydrogen thiosulfate
RefChem:327823
DTXCID20100652
4-[[3-[[2-(Sulfothio)ethyl]amino]propyl]amino]benzoic acid 1-ethyl ester