4-(dihydroxyamino)-N-oxo-benzamide | Solubility of Things

Identification

Molecular formula

C₇H₇N₂O₄

CAS number

115961-06-9

IUPAC name

4-(dihydroxyamino)-N-oxo-benzamide

State

At room temperature, 4-(dihydroxyamino)-N-oxo-benzamide is typically a solid.

Melting point (Celsius)

165.00

Melting point (Kelvin)

438.15

Boiling point (Celsius)

345.00

Boiling point (Kelvin)

618.15

General information

Molecular weight

168.14g/mol

Molar mass

168.1440g/mol

Density

1.4600g/cm³

Appearence

This compound appears as a crystalline solid. The crystals can have a range of colors depending on the level of purity and the precise synthesis method used.

Comment on solubility

Solubility of 4-(Dihydroxyamino)-N-oxo-benzamide

4-(Dihydroxyamino)-N-oxo-benzamide exhibits interesting solubility characteristics that may influence its applications in various fields. Notably, the presence of multiple functional groups, particularly the dihydroxyamino group and the amide group, contributes to its solubility profile.

Solubility Features

Polarity: The hydroxyl groups present in the structure enhance the polarity of the molecule, which typically increases solubility in polar solvents such as water.
Hydrogen Bonding: Ability to form hydrogen bonds due to the –OH and –NH groups enhances its interactions with solvent molecules, further improving solubility.
pH Dependence: The solubility may vary with pH levels due to potential ionization of the amino group, making it more soluble in acidic or alkaline solutions.

In conclusion, due to its unique structural characteristics and the ability to form hydrogen bonds, 4-(dihydroxyamino)-N-oxo-benzamide is expected to be soluble in polar solvents, particularly water. This solubility can be a critical factor when considering its applications in pharmaceuticals and chemical synthesis.

Interesting facts

Interesting Facts About 4-(Dihydroxyamino)-N-oxo-benzamide

4-(Dihydroxyamino)-N-oxo-benzamide is an intriguing compound with notable properties and applications in various fields. Here are some captivating aspects of this chemical:

Functional Group Diversity: This compound contains both a benzamide and a hydroxylamine structure, making it a prime example of compounds that feature functional group diversity. Such structures are often investigated for their potential in pharmaceuticals and agrochemicals.
Biological Activity: Many derivatives of benzamides are known for their biological activities, and this particular compound may show potential in medicinal chemistry. Its structural characteristics suggest it could interact effectively with biological systems.
Research Interest: The compound is of interest for research related to antioxidant properties, as hydroxylamine derivatives can scavenge free radicals, which are implicated in many diseases.
Synthesis Routes: The synthesis of 4-(dihydroxyamino)-N-oxo-benzamide may involve several steps, highlighting the importance of synthetic chemistry techniques. Understanding the synthesis can provide insight into more complex organic reactions.
Potential Applications: Beyond medicinal uses, the compound may find utility in materials science or as a reagent in organic synthesis, making it a versatile addition to a chemist's toolkit.

In summary, 4-(Dihydroxyamino)-N-oxo-benzamide presents a combination of functional diversity and potential utility that continues to pique the interest of scientists. As research progresses, who knows the future applications that may arise from exploring this compound further!