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Phenyl 2-(phenoxycarbonylamino)ethylsulfanylformate

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Identification
Molecular formula
C16H15NO4S
CAS number
34120-56-4
IUPAC name
phenyl 2-(phenoxycarbonylamino)ethylsulfanylformate
State
State

At room temperature, this compound is usually found as a solid. It is stable under standard conditions and will maintain its solid state unless heated to its melting point.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.00
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.00
General information
Molecular weight
317.35g/mol
Molar mass
317.3530g/mol
Density
1.3000g/cm3
Appearence

This compound is typically a white to off-white solid in appearance. It may be found as a powder or crystalline solid, exhibiting a uniform color.

Comment on solubility

Solubility of Phenyl 2-(phenoxycarbonylamino)ethylsulfanylformate

Phenyl 2-(phenoxycarbonylamino)ethylsulfanylformate is a complex organic compound that exhibits notable solubility characteristics. Understanding its solubility is essential for various applications in chemical synthesis and formulation.

Key Solubility Insights

  • Solvent Dependence: This compound shows varied solubility depending on the choice of solvent. It is typically more soluble in polar organic solvents such as methanol and dimethyl sulfoxide (DMSO).
  • Water Solubility: The solubility in water is generally low, which is not uncommon for compounds containing bulky phenyl groups and multi-functional moieties like this one.
  • pH Influence: The solubility may be influenced by pH, particularly because of functional groups that can ionize, potentially enhancing solubility in more acidic or basic conditions.
  • Temperature Effects: Increased temperature often improves solubility, facilitating dissolution of this compound in suitable solvents.

In summary, the solubility of phenyl 2-(phenoxycarbonylamino)ethylsulfanylformate is characterized by its dependence on solvent type, pH levels, and temperature. This behavior is vital for optimizing its use in various chemical processes.

Interesting facts

Interesting Facts about Phenyl 2-(Phenoxycarbonylamino)ethylsulfanylformate

Phenyl 2-(phenoxycarbonylamino)ethylsulfanylformate is a unique compound in the realm of organic chemistry, notable for its multifaceted applications and intriguing structure. Here are some striking points about this compound:

  • Biological Significance: Compounds like this one often find their roles in pharmaceuticals or agrochemicals. Due to its functional groups, it could potentially exhibit biological activities, making it a candidate for drug discovery.
  • Functional Group Diversity: The presence of both carbonyl and aminothioether functionalities in the structure demonstrates the versatility of the compound, allowing for engaging reactivity in synthesis and derivations.
  • Reactivity: The compound may partake in a variety of chemical reactions. Its thiol and amine functionalities suggest that it could react with electrophiles or serve in nucleophilic substitution reactions.
  • Analytical Applications: This compound can be a valuable standard in analytical chemistry, where it may be used in chromatographic methods or as a reference in mass spectrometry to identify and quantify related compounds.
  • Potential in Material Science: Given its structure, there is potential for the utilization of this compound in the development of advanced materials, such as polymers or coatings that require specific functional characteristics.

Additionally, as the field of synthetic organic chemistry continues evolving, compounds like phenyl 2-(phenoxycarbonylamino)ethylsulfanylformate serve as intriguing subjects for academic research and industrial exploration. In the words of a noted chemist, "The complexities of organic compounds are often where the magic of discovery lies." Thus, understanding such compounds can lead to remarkable advancements in science and technology.

Synonyms
BRN 2005105
Carbamic acid, (2-mercaptoethyl)-, phenyl ester, S-ester with phenylthiocarbonate
28174-17-6
Phenyl N-(2-(phenylthiolcarbonate)ethyl) carbamate
Carbamic acid, N-(2-(phenylthiocarbonato)ethyl)-, phenyl ester
DTXSID20182453
RefChem:331955
DTXCID30104944