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(4-Chlorophenyl)thioethyl ethyl thioxophosphane

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Identification
Molecular formula
C8H9ClO2PS
CAS number
3674-41-3
IUPAC name
(4-chlorophenyl)sulfanyl-ethoxy-ethyl-thioxo-lambda5-phosphane
State
State

At room temperature, this compound is in a liquid state. It is usually handled in a controlled laboratory setting due to its potential reactivity and volatility.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
250.68g/mol
Molar mass
250.6800g/mol
Density
1.4200g/cm3
Appearence

The compound appears as a colorless liquid. It might exhibit a slight odor typical of organophosphorus compounds.

Comment on solubility

Solubility of (4-chlorophenyl)sulfanyl-ethoxy-ethyl-thioxo-lambda5-phosphane

The solubility characteristics of (4-chlorophenyl)sulfanyl-ethoxy-ethyl-thioxo-lambda5-phosphane can be intriguing due to its complex molecular structure. Understanding solubility involves examining various factors:

  • Polarity: The presence of both sulfur and phosphorus atoms in the compound may influence its overall polarity. Generally, compounds with higher polarity tend to be more soluble in polar solvents, such as water.
  • Molecular Interactions: The electron-withdrawing effect of the 4-chlorophenyl group may enhance solubility by facilitating interactions with solvent molecules.
  • Functional Groups: The ethoxy group can contribute to solubility in organic solvents due to its hydrophobic nature, potentially leading to varied solubility in different media.
  • Temperature Effects: The solubility is expected to vary with temperature; typically, increased temperature can lead to enhanced solubility for many organic compounds.

In particular, this compound might exhibit:

  1. Moderate solubility in organic solvents.
  2. Possibly lower solubility in water due to its non-polar characteristics.

In summary, while the precise solubility profile of (4-chlorophenyl)sulfanyl-ethoxy-ethyl-thioxo-lambda5-phosphane would require experimental determination, the interplay of its molecular features suggests an intriguing behavior in various solvents.

Interesting facts

Interesting Facts about (4-Chlorophenyl)sulfanyl-ethoxy-ethyl-thioxo-lambda5-phosphane

(4-Chlorophenyl)sulfanyl-ethoxy-ethyl-thioxo-lambda5-phosphane is an intriguing organophosphorus compound that exhibits a range of interesting properties and potential applications. Here are some noteworthy facts:

  • Functional Group Riche: This compound boasts multiple functional groups, combining both sulfur and phosphorus chemistry. The presence of the thioxo group (≥C=S) in this molecule enhances its reactivity, offering valuable insights for various chemical reactions.
  • Biological Activity: Organophosphorus compounds, similar to this one, can exhibit biological significance. Many such compounds have been researched for their potential as agrochemicals or pharmaceuticals, highlighting the ongoing interest in their bioactivity.
  • Versatile Applications: Due to its unique structure, (4-Chlorophenyl)sulfanyl-ethoxy-ethyl-thioxo-lambda5-phosphane can be explored for applications ranging from drug development to the creation of new materials. Its complex framework can inspire innovative approaches in synthetic organic chemistry.
  • Chlorophenyl Influence: The 4-chlorophenyl group attached to the phosphane adds considerable influence on the compound's chemical behavior. Chlorinated aromatic compounds are known for their ability to alter solubility and reactivity, thus providing new pathways for synthesis and use.
  • Lambda5-Phosphane Characteristic: The lambda5-phosphane notation indicates the oxidation state of phosphorus in this compound, which contributes to its reactivity and interaction with other substances. Understanding this aspect is crucial when considering its chemical properties.

In summary, (4-Chlorophenyl)sulfanyl-ethoxy-ethyl-thioxo-lambda5-phosphane is a remarkable compound that exemplifies the intersection of sulfur, phosphorus, and organic chemistry. As research progresses, it may uncover even more hidden potential in various fields.

Synonyms
Stauffer N-2596
2984-64-7
Bayer 36743
BAY 36743
N-2596
ENT 25,723
BRN 1971198
AI3-25723
O-Ethyl S-4-chlorophenyl ethylphosphonodithioate
S-(p-Chlorophenyl) O-ethyl ethanephosphonodithioate
Phosphonodithioic acid, ethyl-, S-(4-chlorophenyl) O-ethyl ester
Phosphonodithioic acid, ethyl-, S-(p-chlorophenyl) O-ethyl ester
O-ethyl S-4-chlorophenylethanephosphonodithioate
N 2596
S-(4-Chlorophenyl) O-ethyl ethylphosphonodithioate
(4-chlorophenyl)sulfanyl-ethoxy-ethyl-sulfanylidene-lambda5-phosphane
SCHEMBL7844145
DTXSID00952292
O-ethyl S-4-chlorophenyl ethanephosphonodithioate
Ethylphosphonodithioic acid, S-(4-chlorophenyl) O-ethyl ester