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Identification
Molecular formula
C9H18NO4P
CAS number
2104-64-5
IUPAC name
4-ethyl-2,6,7-trioxa-1lambda5-phosphabicyclo[2.2.2]octane 1-oxide
State
State

This compound is generally in a liquid state at room temperature due to its relatively low melting point and high boiling point.

Melting point (Celsius)
-36.00
Melting point (Kelvin)
237.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
221.20g/mol
Molar mass
221.2040g/mol
Density
1.3500g/cm3
Appearence

The compound appears as a colorless to pale yellow liquid with a characteristic odor. It is typically clear and free of particulate matter.

Comment on solubility

Solubility of 4-ethyl-2,6,7-trioxa-1lambda5-phosphabicyclo[2.2.2]octane 1-oxide

When discussing the solubility of 4-ethyl-2,6,7-trioxa-1lambda5-phosphabicyclo[2.2.2]octane 1-oxide, it is important to consider several factors that influence its behavior in various solvents. Generally, the solubility of a compound is dictated by its molecular structure and the nature of the solvent. Here are some key aspects to take into account:

  • Polarity: The presence of oxygen and phosphorus atoms in this compound suggests it may exhibit polar characteristics, likely increasing its solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds due to the oxygen atoms can enhance solubility in protic solvents.
  • Molecular Interactions: Van der Waals forces and dipole-dipole interactions may play a role in the solubility, particularly with organic solvents.
  • Concentration: The solubility of solid forms of this compound may vary significantly with concentration, possibly leading to saturation points in specific solvents.

It is often stated that "like dissolves like," so understanding the chemical nature of both the solute and solvent is vital for predicting solubility outcomes. For instance, if attempting to dissolve 4-ethyl-2,6,7-trioxa-1lambda5-phosphabicyclo[2.2.2]octane 1-oxide in a non-polar solvent, one might encounter limited solubility due to inadequate interaction forces.

Ultimately, the solubility of this compound can be multifaceted, influenced by various physicochemical properties that warrant further experimental investigation to ascertain precise solubility limits under different conditions.

Interesting facts

Interesting Facts about 4-ethyl-2,6,7-trioxa-1lambda5-phosphabicyclo[2.2.2]octane 1-oxide

4-ethyl-2,6,7-trioxa-1lambda5-phosphabicyclo[2.2.2]octane 1-oxide is a fascinating compound that belongs to a unique category of organophosphorus chemistry. Here are some engaging insights about this intriguing molecule:

  • Structural Complexity: This compound features a bicyclic structure, which is characteristic of many complex organic molecules. The incorporation of both sulfur and oxygen into its framework allows for unique reactivity and interactions.
  • Applications: Organophosphorus compounds, like this one, have found important roles in various fields such as agriculture, pharmaceuticals, and materials science. Their diverse applications stem from the versatility of phosphorus in forming stable compounds.
  • Environmental Impact: Understanding phosphorous compounds is crucial as they can influence environmental processes. Studies on their degradation can help assess their potential ecological effects.
  • Historical Significance: Research into phosphorus chemistry dates back to the 17th century, and it has greatly advanced since then, making compounds like this one essential for modern chemistry.

As chemists explore the boundaries of nomenclature and compound design, 4-ethyl-2,6,7-trioxa-1lambda5-phosphabicyclo[2.2.2]octane 1-oxide exemplifies the intricate interplay of various elements forming stable and functional compounds, driving research and innovation in chemical applications.

Synonyms
1005-93-2
ETBICYPHAT
TRIMETHYLOLPROPANE PHOSPHATE
Ethyl bicyclic phosphate
2,6,7-Trioxa-1-phosphabicyclo[2.2.2]octane, 4-ethyl-, 1-oxide
TMP-P
Trimethylopropane phosphate
Trimethyolpropane phosphate
4-Ethyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane 1-oxide
1,1,1-Trimethylolpropane Phosphate
2-(Hydroxymethyl)-2-ethyl-1,3-propanediol, cyclic phosphate (1:1)
2-Ethyl-2-(hydroxymethyl)-1,3-propanediol, cyclic phosphate (1:1)
4-ethyl-2,6,7-trioxa-1lambda5-phosphabicyclo[2.2.2]octane 1-oxide
4-Ethyl-1-phospha-2,6,7-trioxabicyclo(2.2.2)octane-1-oxide
1,3-Propanediol, 2-ethyl-2-(hydroxymethyl)-, cyclic phosphate
NSC-72890
4-Aethyl-1-phospha-2,6,7-trioxabicyclo(2.2.2)octan-1-oxid
4-Ethyl-2,6,7-trioxa-1-phosphabicyclo(2.2.2)octane-1-oxide
2,6,7-Trioxa-1-phosphabicyclo(2.2.2)octane, 4-ethyl-, 1-oxide
4-Ethyl-2,6,7-trioxa-1-phosphabicyclo(2.2.2)octane 1-oxide
2,6,7-Trioxa-1-phosphabicyclo-[2.2.2]octane, 4-ethyl-, 1-oxide
EINECS 213-740-6
BRN 1909748
4-Ethyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane-1-oxide
2,6,7-Trioxa-1-phosphabicyclo-(2.2.2)octane, 4-ethyl-, 1-oxide
starbld0009575
1-Ethyl-1-phospha-2,6,7-trioxabicyclo(2.2.2)octane 1-oxide
1-Ethyl-1-phospha-2,6,7-trioxabicyclo(2.2.2)octane-1-oxide
4-Ethyl-1-phospha-2,6,7 trioxabicyclo(2.2.2)octane-1-oxide
4-Aethyl-1-phospha-2,6,7-trioxabicyclo(2.2.2)octan-1-oxid [German]
5ZYS7J5LT3
SCHEMBL813272
DTXSID5058270
4-ethyl-1-phospha-2,6,7-trioxabicyclo(2.2.2.)octane-1-oxide
NSC72890
Etbicyphat, >=95% (NMR), solid
MFCD00043597
NSC 72890
AKOS006272342
WLN: T4PTJ AO BQ C2Q C1 DQ
DA-49706
HY-139145
NS00005121
F82933
1, 2-ethyl-2-(hydroxymethyl)-, cyclic phosphate
1, 2-ethyl-2-(hydroxymethyl)-, cyclic phosphate (1:1)
4-Aethyl-1-phospha-2,7-trioxabicyclo[2.2.2]octan 1-oxid
4-Ethyl-1-phospha-2,7-trioxabicyclo[2.2.2]octane 1-oxide
4-ethyl-2,6,7-trioxa-1-phosphabicy-clo[2.2.2]octane 1-oxide
4-ethyl-2,6,7-trioxa-1|E?-phosphabicyclo[2.2.2]octan-1-one
4-Ethyl-2,7-trioxa-1-phosphabicyclo[2.2.2]octane 1-oxide
2,7-Trioxa-1-phosphabicyclo[2.2.2]octane, 4-ethyl-, 1-oxide
2-Ethyl-2-(hydroxymethyl)-1,3-propanediol cyclic phosphate (1:1)
4-ETHYL-2,6,7-TRIOXA-1??-PHOSPHABICYCLO[2.2.2]OCTAN-1-ONE