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Diallyl phosphorothioate

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Identification
Molecular formula
C6H11O2PS
CAS number
90-43-7
IUPAC name
diallyloxy-sulfanyl-thioxo-lambda5-phosphane
State
State

At room temperature, diallyl phosphorothioate is typically in a liquid state. It remains stable under normal conditions but should be handled with caution due to its potential toxic effects.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
255.50
Boiling point (Kelvin)
528.65
General information
Molecular weight
188.20g/mol
Molar mass
188.2000g/mol
Density
1.1400g/cm3
Appearence

Diallyl phosphorothioate is typically a colorless to pale yellow liquid. Its appearance can sometimes be oily, and it is recognized for its potent garlic-like odor, which is characteristic of organophosphorus compounds.

Comment on solubility

Solubility of Diallyloxy-sulfanyl-thioxo-lambda5-phosphane

Diallyloxy-sulfanyl-thioxo-lambda5-phosphane is a unique chemical compound whose solubility characteristics are of significant interest. Solubility can often be influenced by various factors, leading to diverse observations:

  • Polar vs. Nonpolar Solvents: This compound is likely to exhibit varying solubility in polar and nonpolar solvents due to its functional groups. The presence of sulfur and phosphorus could enhance solubility in polar environments.
  • Temperature Dependencies: As with many chemical compounds, solubility may increase with temperature. Consequently, conducting solubility tests at different temperatures could provide valuable insights.
  • pH Impact: The solubility of thioxo compounds can be sensitive to pH levels. Given that diallyloxy-sulfanyl-thioxo-lambda5-phosphane has sulfur and phosphorus, it may behave differently in acidic or basic solutions.
  • Concentration Effects: When dissolved in a solvent, the concentration can affect solubility limits, leading to saturation where further dissolution becomes impossible.

While definitive solubility data may be limited, it is essential to recognize that the interaction of this compound with solvents can lead to interesting results. Striking a balance between solubility and the conditions of the environment, such as temperature and pH, will yield the most informative observations. It is an area ripe for exploration, posing questions that can guide future research.

Interesting facts

Diallyloxy-sulfanyl-thioxo-lambda5-phosphane

Diallyloxy-sulfanyl-thioxo-lambda5-phosphane is a fascinating chemical compound that opens doors to various applications and research opportunities in the fields of organophosphorus chemistry and materials science. Here are some intriguing aspects about this compound:

  • Unique Structure: Its structure features a phosphorous atom bound to both sulfur and oxygen atoms, showcasing the fascinating versatility of phosphorous compounds in organic synthesis.
  • Synthetic Versatility: The incorporation of allyl groups indicates potential for further reactions, as the double bonds can participate in various chemical transformations, making it a valuable intermediate.
  • Potential Applications: Research explores its potential in pesticides, flame retardants, and as ligands in coordination chemistry, demonstrating its importance in diverse industrial applications.
  • Reactivity: The thioxo group (–S=O) can provide interesting reactivity patterns in nucleophilic additions and substitutions, paving the way for novel synthesis pathways.
  • Research Interest: As a relatively lesser-known compound, it attracts attention from chemists intrigued by the properties and behaviors of sulfur-containing phosphorous compounds.

In conclusion, diallyloxy-sulfanyl-thioxo-lambda5-phosphane exemplifies the richness of organophosphorus chemistry and serves as a reminder of the importance of exploring lesser-known compounds that might hold the key to innovative applications and discoveries. Its fascinating combination of elements and functional groups continues to inspire chemistry enthusiasts!

Synonyms
5851-14-9
O,O-DIALLYL DITHIOPHOSPHATE
SCHEMBL30824
DTXSID10974066
O,O'-diallyldithiophosphoric acid
O,O-Diprop-2-en-1-yl hydrogen phosphorodithioate