Methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate

Identification

Molecular formula

C₁₁H₁₈ClO₆P

CAS number

IUPAC name

methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate

State

At room temperature, methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate is in a liquid state.

Melting point (Celsius)

-25.00

Melting point (Kelvin)

248.15

Boiling point (Celsius)

289.00

Boiling point (Kelvin)

562.15

General information

Molecular weight

322.73g/mol

Molar mass

322.7270g/mol

Density

1.2789g/cm³

Appearence

This compound generally appears as a colorless to pale yellow liquid. It has a faint, characteristic odor.

Comment on solubility

Solubility of Methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate

The solubility of methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate can be influenced by several key factors:

Polarity: This compound features both polar and non-polar functional groups, which can lead to mixed solubility properties.
Solvation: The presence of the phosphoryl group can enhance interactions with polar solvents, potentially increasing solubility in polar media like water.
Hydrophobic Interactions: The chloropropoxy and isopropoxy branches may introduce hydrophobic characteristics, which could limit solubility in highly polar solvents.
Temperature: Higher temperatures may increase solubility due to kinetic energy overcoming intermolecular forces.

It is essential to consider the following:

The compound is likely to be soluble in organic solvents such as acetone or ethanol.
In water, the solubility can be moderate, mainly due to the presence of the polar phosphoryl group.

In conclusion, understanding the solubility of methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate is vital for its application in various chemical processes, and modifications of solvent properties can help optimize its use.

Interesting facts

Interesting Facts about Methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate

Methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate is a fascinating compound that falls within the realm of organophosphate chemistry. Here are some notable aspects to consider:

Versatile Applications: This compound is characterized by its multifunctional properties, which makes it a promising candidate for various applications in agriculture, particularly as a pesticide.
Phosphoryl Group: The presence of a phosphoryl group plays a crucial role in its biological activity, enabling interactions with enzymatic systems in living organisms.
Chlorine Substituent: The chlorine atom enhances the lipophilicity of the compound, impacting its permeability and absorption in biological systems.
Synthesis Challenges: The synthesis of this compound can involve complex reactions, often requiring specific conditions and catalysts to achieve desired yields.
Environmental Considerations: As with many organophosphates, understanding the environmental fate and degradation pathways of this compound is critical for assessing its ecological impact.

As a chemical student studying such compounds, it's essential to appreciate their intricate structures and dynamics. Engaging with their synthesis and reactivity helps develop valuable skills for future research and applications in medicinal or agricultural chemistry.

In the words of renowned chemist Linus Pauling, "Scientific research is one of the most exciting and rewarding of human activities." Embrace the challenge of studying compounds like methyl 3-[2-chloropropoxy(isopropoxy)phosphoryl]oxybut-2-enoate, as they provide insight into the delicate balance between chemistry, utility, and safety.