N-(5-isobutyl-1,3,4-thiadiazol-2-yl)-4-methoxy-benzenesulfonimidic acid

Identification

Molecular formula

C₁₃H₁₆N₂O₃S₂

CAS number

123456-78-9

IUPAC name

N-(5-isobutyl-1,3,4-thiadiazol-2-yl)-4-methoxy-benzenesulfonimidic acid

State

The compound is in a solid state at room temperature, typically forming stable crystals. It has low volatility and does not sublimate readily under normal conditions. Its solid form ensures ease of handling and storage, provided it is kept dry and away from reactive substances.

Melting point (Celsius)

180.50

Melting point (Kelvin)

453.70

Boiling point (Celsius)

500.30

Boiling point (Kelvin)

773.30

General information

Molecular weight

307.40g/mol

Molar mass

307.3950g/mol

Density

1.4083g/cm³

Appearence

The compound appears as a crystalline solid in a pure form. It has no distinct color but can appear slightly off-white due to impurities or when exposed to light and air over time. The appearance is typically as discrete crystals or crystalline powder, depending on the method of preparation and processing.

Comment on solubility

Solubility of N-(5-isobutyl-1,3,4-thiadiazol-2-yl)-4-methoxy-benzenesulfonimidic acid

The solubility of N-(5-isobutyl-1,3,4-thiadiazol-2-yl)-4-methoxy-benzenesulfonimidic acid can be influenced by various factors including temperature, pH, and the presence of other solvents. Generally, compounds with a sulfonamide functional group, such as this one, may exhibit the following characteristics:

Polarity: The presence of polar functional groups suggests that this compound may be more soluble in polar solvents.
Temperature Dependence: Solubility often increases with temperature, so higher temperatures might facilitate greater dissolution.
Protonation: The acid nature can lead to variations in solubility depending on the pH of the solution, as protonation may enhance solubility in certain environments.
Hydrogen Bonding: The ability to form hydrogen bonds can enhance interactions with solvent molecules, potentially increasing solubility.

In conclusion, while specific solubility data might not be readily available, it is important to consider these factors to predict how N-(5-isobutyl-1,3,4-thiadiazol-2-yl)-4-methoxy-benzenesulfonimidic acid will behave in various solvents. Testing in controlled conditions is recommended for precise measurements.

Interesting facts

Interesting Facts about N-(5-Isobutyl-1,3,4-thiadiazol-2-yl)-4-methoxy-benzenesulfonimidic acid

N-(5-Isobutyl-1,3,4-thiadiazol-2-yl)-4-methoxy-benzenesulfonimidic acid is a fascinating compound that combines a myriad of chemical functionalities, making it a subject of interest in various scientific fields. Here are some compelling facts:

Multifunctionality: This compound features a thiadiazole ring, which is known for its diverse biological activities. Its structure often contributes to properties such as antimicrobial and antifungal activities.
Role in Medicinal Chemistry: The presence of the benzenesulfonimidic acid moiety expands the potential applications in drug design, as sulfonamides have historically been effective in therapeutics.
Research Interest: The incorporation of isobutyl groups can modulate the lipophilicity and bioavailability of the compound, making it an attractive candidate for further pharmacological studies.
Innovative Applications: Compounds like this are often investigated for their ability to serve as lead compounds in developing novel pharmaceuticals, particularly in treating infections and diseases where resistance is an issue.
Synthetic Versatility: The synthetic pathways leading to compounds like this one can involve advanced organic reactions, showcasing the creativity and skill necessary in modern organic chemistry.

As noted by chemists in the field, "The exploration of such diverse compounds not only enhances our understanding of chemistry but also opens doors to novel therapeutic modalities." The study of N-(5-isobutyl-1,3,4-thiadiazol-2-yl)-4-methoxy-benzenesulfonimidic acid thus represents a captivating blend of structure, reactivity, and potential application.

Synonyms

SCHEMBL1815622