2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enimidothioic acid

Identification

Molecular formula

C₁₀H₈N₂O₃S

CAS number

IUPAC name

2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enimidothioic acid

State

At room temperature, it exists in a solid state.

Melting point (Celsius)

150.00

Melting point (Kelvin)

423.00

Boiling point (Celsius)

250.00

Boiling point (Kelvin)

523.00

General information

Molecular weight

192.27g/mol

Molar mass

192.2690g/mol

Density

1.4000g/cm³

Appearence

This compound typically appears as a yellowish crystalline powder.

Comment on solubility

Solubility of 2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enimidothioic acid

The solubility of 2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enimidothioic acid (C₁₀H₈N₂O₃S) is influenced by several key factors:

Polarity: The presence of hydroxyl (-OH) groups in the compound enhances its polarity, which may increase solubility in polar solvents like water.
Functional Groups: The cyano (-C≡N) and thioic acid (-S) functional groups can contribute to solubility changes in various solvents, especially in organic solvents.
pH Levels: The solubility can be affected by the pH of the solution; in more alkaline or acidic solutions, ionization of functional groups could occur, enhancing solubility.
Hydrogen Bonding: The ability of the compound to form hydrogen bonds with water molecules may also play a crucial role in its solubility profile.

As a result, while 2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enimidothioic acid might exhibit **moderate solubility** in polar solvents, its behavior in non-polar solvents is expected to be vastly different. Understanding these parameters is essential for practical applications, as stated, "Solubility is the gateway to bioavailability."

In essence, the solubility of this compound is a multifaceted characteristic that can vary widely based on environmental and chemical conditions.

Interesting facts

Interesting Facts About 2-Cyano-3-(3,4-dihydroxyphenyl)prop-2-enimidothioic Acid

2-Cyano-3-(3,4-dihydroxyphenyl)prop-2-enimidothioic acid is a fascinating compound that showcases the intricate chemistry found within organic molecules. Here are some compelling insights about this compound:

Diverse Functional Groups: This compound features multiple functional groups, including a cyano group (-C≡N), which is known for its ability to participate in a wide array of chemical reactions, including nucleophilic additions and cycloadditions.
Potential Biological Activities: Compounds with similar structures have been investigated for their biological activities, including antimicrobial and antioxidant properties. The presence of hydroxyl groups may enhance its potential for therapeutic applications.
Thioic Acid Derivative: As a thioic acid derivative, this compound may exhibit unique chemical behaviors. Thioic acids are generally known for their reactivity due to the sulfur atom, which can engage in various inter- and intramolecular interactions.
Applications in Material Science: The structural attributes of this compound, particularly its conjugated system, suggest possible applications in material science, such as in the development of new sensors or organic semiconductors.
Research Potential: The intricate structure opens avenues for research in synthetic chemistry, offering potential pathways for creating novel derivatives with tailored properties.

In sum, 2-cyano-3-(3,4-dihydroxyphenyl)prop-2-enimidothioic acid not only exemplifies the complexity of organic compounds but also hints at the versatility and potential of its diverse functional groups. As a subject of study, it can lead to exciting discoveries in both chemistry and biology!