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2-ethoxyethyl-(p-tolyl)-sulfanyl-thioxo-λ5-phosphane

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Identification
Molecular formula
C11H17O2PS
CAS number
No CAS number found
IUPAC name
2-ethoxyethyl-(p-tolyl)-sulfanyl-thioxo-lambda5-phosphane
State
State

At room temperature, this compound is typically found in a liquid state. It possesses higher viscosity compared to simple hydrocarbons and exhibits moderate purity stability.

Melting point (Celsius)
-4.00
Melting point (Kelvin)
269.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
256.34g/mol
Molar mass
256.3410g/mol
Density
1.3200g/cm3
Appearence

The compound is expected to appear as a pale yellow to light brown liquid. Such organophosphorus compounds generally have a characteristic odor due to the presence of sulfur and phosphorus elements.

Comment on solubility

Solubility of 2-ethoxyethyl-(p-tolyl)-sulfanyl-thioxo-lambda5-phosphane

The solubility of 2-ethoxyethyl-(p-tolyl)-sulfanyl-thioxo-lambda5-phosphane in various solvents can be quite intriguing. This compound, characterized by its unique structure, exhibits diverse solubility properties that depend significantly on the solvent used. Here are some key points regarding its solubility:

  • Polar solvents: It is expected that this compound shows higher solubility in polar solvents due to the presence of the ether group which enhances interactions via hydrogen bonding.
  • Non-polar solvents: Conversely, its solubility in non-polar solvents might be limited, given that the large aromatic p-tolyl group can lead to reduced affinities.
  • Temperature effects: Temperature could also play a crucial role, with increased temperatures generally promoting solubility, especially in organic solvents.
  • Functional groups impact: The presence of both sulfur and phosphorus atoms can lead to interesting solubility dynamics, potentially influencing the compound's reactivity and interactions in solution.

In conclusion, while specific solubility data might not be readily available, understanding the underlying factors that contribute to the solubility of 2-ethoxyethyl-(p-tolyl)-sulfanyl-thioxo-lambda5-phosphane allows for greater predictability in its behavior within various chemical contexts. As with many complex compounds, conducting empirical studies in different solvents will yield the most definitive insights.

Interesting facts

Interesting Facts about 2-ethoxyethyl-(p-tolyl)-sulfanyl-thioxo-lambda5-phosphane

This intriguing compound is a member of the phosphane family, known for its unique properties and applications in various chemical processes. Here are some fascinating aspects about this compound:

  • Diverse Applications: 2-ethoxyethyl-(p-tolyl)-sulfanyl-thioxo-lambda5-phosphane plays a critical role in organic synthesis and catalysis. Its unique structure allows it to act as a ligand in coordination chemistry and as a reagent in nucleophilic substitutions.
  • Phosphorus Chemistry: Phosphorus compounds like this one are vital in the study of organophosphorus chemistry, where understanding their behavior can lead to innovations in materials science, agriculture, and pharmaceuticals.
  • Thioxo Group: The presence of a thioxo group introduces interesting properties to this compound, giving it potential applications in developing new surface-active agents, particularly in the field of surfactants and emulsifiers.
  • Environmental Impact: Some phosphane compounds are known to possess specific biological activities, making them valuable in environmental chemistry. Studies are ongoing to assess the impact of such compounds on ecosystems and their utility in remediation techniques.

The synthesis of this compound often involves elaborate multi-step processes, showcasing the creativity and precision necessary in modern chemistry. As scientists continue to explore its potential, this compound embodies the intersection of theoretical study and practical application in the world of chemical science.

Synonyms
Stauffer N-2788
(2-ethoxyethyl)(4-methylphenyl)phosphinodithioic acid
O-Ethyl S-p-tolyl ethylphosphonodithioate
BAYER 38156
BAY 38156
ENT 25713
BRN 2647740
AI3-25713
N 2788
S 4706
Phosphonodithioic acid, ethyl-, O-ethyl S-(p-tolyl) ester
XJPQQYILDIYJHE-UHFFFAOYSA-N
O-Ethyl-S-p-tolylester kyseliny ethyldithiofosfonove [Czech]
p-Toluenethiol, S-ester with O-ethyl ethylphosphonodithioate
NS00126630
O-Ethyl-S-p-tolylester kyseliny ethyldithiofosfonove