4-(2-Hydroxyphenyl)sulfanylbut-1-enylphosphonic acid

Identification

Molecular formula

C₁₀H₁₃O₄PS

CAS number

None

IUPAC name

4-(2-hydroxyphenyl)sulfanylbut-1-enylphosphonic acid

State

The compound is found in a solid state at room temperature. It is stable under normal conditions but should be stored in a cool, dry place to avoid decomposition.

Melting point (Celsius)

150.00

Melting point (Kelvin)

423.15

Boiling point (Celsius)

290.00

Boiling point (Kelvin)

563.15

General information

Molecular weight

244.31g/mol

Molar mass

244.3060g/mol

Density

1.4600g/cm³

Appearence

The compound typically presents as a solid crystalline powder. The appearance can vary slightly depending on the method of synthesis and the degree of purity, but it is generally a white to off-white solid.

Comment on solubility

Solubility of 4-(2-hydroxyphenyl)sulfanylbut-1-enylphosphonic acid

The solubility of 4-(2-hydroxyphenyl)sulfanylbut-1-enylphosphonic acid (C₁₀H₁₃O₄PS) is an intriguing aspect of its chemical behavior. This compound contains several functional groups that influence its ability to dissolve in various solvents.

Key factors affecting its solubility include:

Functional Groups: The presence of the phosphonic acid group increases hydrophilicity, potentially enhancing solubility in polar solvents like water.
Hydroxyl Groups: The –OH groups facilitate hydrogen bonding, which generally contributes to increased solubility in aqueous environments.
Length of the Aliphatic Chain: The butenyl portion may introduce some hydrophobic character, possibly limiting solubility in highly polar solvents.

In general, it is expected that:

4-(2-hydroxyphenyl)sulfanylbut-1-enylphosphonic acid will exhibit significant solubility in polar solvents due to the phosphonic acid and hydroxyl groups.
It may have lower solubility in non-polar solvents due to the hydrophobic influences of the butenyl chain.

Overall, the solubility profile of this compound indicates a distinct balance between polar and non-polar characteristics, making it a compound of interest for further investigation in various chemical environments.

Interesting facts

Interesting Facts about 4-(2-hydroxyphenyl)sulfanylbut-1-enylphosphonic acid

This intriguing compound is known for its multifaceted applications in the field of chemistry, particularly in the realm of biochemistry and agricultural science. Here are some noteworthy points to consider:

Phosphonic acid derivatives: As a phosphonic acid derivative, it plays a crucial role in studies related to phosphonate chemistry, which is significant for understanding bacterial metabolism and soil chemistry.
Biological significance: Compounds like 4-(2-hydroxyphenyl)sulfanylbut-1-enylphosphonic acid are investigated for their potential as herbicides or plant growth regulators, making them essential in enhancing agricultural productivity.
Antioxidant properties: The presence of the hydroxyl group and sulfur moiety suggests potential antioxidant activity, which is beneficial in various biotechnological applications.
Interaction with biological targets: Research indicates that phosphonic acids can effectively mimic natural phosphates, allowing them to interact with enzyme systems in plants and microbes.

As a final note, this compound exemplifies how synthetic chemistry can intersect with natural processes, opening doors to innovative solutions in environmental and agricultural chemistry. Exploring its functionality beyond traditional applications continues to be an exciting frontier for researchers.

Synonyms

Phosphonic acid, [4-[(2-hydroxyphenyl)thio]-1-butenyl]-

191411-86-6

DTXSID00274325

PD036622