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Dibenzylaminoethyl disulfide

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Identification
Molecular formula
C18H22O2S
CAS number
4506-62-3
IUPAC name
N-[2-[3-(dimethylamino)propylsulfanyl]phenyl]-3-phenyl-prop-2-enamide
State
State

The compound is typically in a solid state at room temperature, often appearing as a crystalline or powdery substance.

Melting point (Celsius)
127.50
Melting point (Kelvin)
400.65
Boiling point (Celsius)
567.90
Boiling point (Kelvin)
841.05
General information
Molecular weight
355.52g/mol
Molar mass
355.5160g/mol
Density
1.1890g/cm3
Appearence

The compound appears as a solid with distinctive crystalline structure. It may vary in color but typically presents in off-white or pale yellow hues.

Comment on solubility

Solubility of N-[2-[3-(dimethylamino)propylsulfanyl]phenyl]-3-phenyl-prop-2-enamide

The solubility of N-[2-[3-(dimethylamino)propylsulfanyl]phenyl]-3-phenyl-prop-2-enamide (C18H22O2S) is influenced by its chemical structure, which introduces a range of solvation characteristics. Here are some key points to consider regarding its solubility:

  • Polarity: The presence of the dimethylamino group and the sulfanyl moiety suggest that the compound has certain polar characteristics, which can enhance solubility in polar solvents.
  • Hydrophobic Interactions: The multiple phenyl groups can contribute to hydrophobic interactions. This may limit solubility in highly polar solvents, while favoring solubility in organic solvents like ethanol or acetone.
  • pH Dependency: Solubility may vary with pH due to potential ionization of the amine group, promoting different solubility profiles in aqueous environments.
  • Temperature Effects: As with many organic compounds, solubility can increase with temperature, so understanding its thermal properties can provide insight into its solubility behavior.

In summary, while the solubility of this compound may exhibit variations based upon environmental conditions, the intricate balance of its hydrophobic and hydrophilic properties plays a pivotal role in determining how it interacts with solvents. Understanding these characteristics is critical for both laboratory synthesis and practical applications.

Interesting facts

Interesting Facts about N-[2-[3-(dimethylamino)propylsulfanyl]phenyl]-3-phenyl-prop-2-enamide

N-[2-[3-(dimethylamino)propylsulfanyl]phenyl]-3-phenyl-prop-2-enamide is a fascinating compound that presents both a challenge and excitement for chemists. Here are some noteworthy aspects:

  • Pharmacological Potential: This compound has garnered interest in the pharmaceutical industry due to its potential applications. Its unique structure suggests it could have significant biological activity, which warrants further investigation.
  • Diverse Functional Groups: The presence of a dimethylamino group and a sulfanyl moiety enables the compound to exhibit diverse interactions within biological systems. Compounds with such groups are often studied for their reactivity and ability to form bonds with various biological targets.
  • Synthetic Versatility: The synthesis of this compound involves multiple steps, highlighting the importance of synthetic chemistry in building complex molecular architectures. Chemists enjoy the challenge of devising efficient routes to produce such structures.
  • Research Interest: Ongoing research may explore the effects of substituents on the compound's activity. As noted in various studies, “modifications to the amide bond can influence the compound's pharmacodynamics and pharmacokinetics,” leading to exciting developments in medicinal chemistry.
  • Potential for Innovation: Given its composition, further exploration into this compound may reveal new pathways for drug discovery, offering solutions to currently unmet medical needs.

In summary, N-[2-[3-(dimethylamino)propylsulfanyl]phenyl]-3-phenyl-prop-2-enamide represents an excellent example of how complex organic compounds can lead to significant advancements in science and medicine. The intersection of synthetic capability and biological potential makes it a compound to watch in future research endeavors.

Synonyms
TCMDC-125843
N-(2-((3-(Dimethylamino)propyl)thio)phenyl)-3-phenylacrylamide
CHEMBL533822
2'-(3-dimethylaminopropylthio) cinnamanilide
Q27164041
N-[2-[3-(dimethylamino)propylthio]phenyl]-3-phenyl-2-propenamide