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Benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonyl-piperazine-1-carboxylate

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Identification
Molecular formula
C19H22N2O6
CAS number
90729-43-4
IUPAC name
benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonyl-piperazine-1-carboxylate
State
State

At room temperature, this compound is typically found in a solid state. It is stable under normal conditions when stored away from moisture and light.

Melting point (Celsius)
102.00
Melting point (Kelvin)
375.15
Boiling point (Celsius)
253.00
Boiling point (Kelvin)
526.15
General information
Molecular weight
332.37g/mol
Molar mass
332.3730g/mol
Density
1.3180g/cm3
Appearence

This compound typically appears as a white to off-white crystalline powder. Its appearance can be affected by the presence of impurities, but in its pure form, it is generally free-flowing.

Comment on solubility

Solubility Overview of Benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonyl-piperazine-1-carboxylate

The solubility of a chemical compound is a critical property that affects its bioavailability, reactivity, and overall functionality in various applications. For the compound benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonyl-piperazine-1-carboxylate (C19H22N2O6), a few important considerations regarding its solubility can be summarized as follows:

  • Polarity: The presence of functional groups such as a hydroxyl group and a sulfonyl group typically enhances polarity, suggesting that the compound may have reasonable solubility in polar solvents such as water.
  • Hydrogen Bonding: The hydroxy and amide functionalities could facilitate hydrogen bonding, which can contribute to solubility in aqueous environments.
  • Molecular Size and Structure: With a relatively large molecular size, high steric hindrance might limit the extent of solubility in some organic solvents.
  • Solvent Choice: It is likely to be more soluble in solvents that can disrupt intermolecular forces, such as DMSO or ethanol, rather than non-polar solvents like hexane.

In summary, while the specific solubility data for this compound may vary, the interactions of functional groups play a pivotal role in determining its overall solubility profile. As emphasized by the proverb, "Like dissolves like," understanding the nature of the solvent can significantly aid in predicting the solubility behavior of benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonyl-piperazine-1-carboxylate.

Interesting facts

Interesting Facts about Benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonyl-piperazine-1-carboxylate

Benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonyl-piperazine-1-carboxylate is a fascinating compound with numerous potential applications in the field of medicinal chemistry. Here are some key points that highlight its importance and uniqueness:

  • Versatile Structure: This compound features a complex structure that combines various functional groups, including a piperazine ring, which is well-known for its pharmacological properties.
  • Potential Therapeutic Applications: Compounds like this one are often studied for their potential in treating a range of conditions, including neurological disorders and cancer, due to the activity of piperazine derivatives in biological systems.
  • Innovative Synthesis: The preparation of such compounds often involves employing advanced synthetic strategies, showcasing the creativity and skill required in medicinal chemistry.
  • Research Implications: This compound may serve as a lead or reference molecule in ongoing research to develop novel therapeutic agents, making it an exciting area of study for both researchers and students.
  • Functional Diversity: The presence of multiple functional groups allows for possible modifications to improve efficacy and reduce side effects in drug design.

The exploration of compounds like benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonyl-piperazine-1-carboxylate opens up numerous avenues for innovation in drug discovery and development. As research continues, this compound may play a significant role in the search for new and effective therapies in modern medicine.

Synonyms
CHEMBL332134
mmp-9/mmp-13 inhibitor ii
SCHEMBL2680478
BDBM50084744
NSC727679
NSC-727679
4-(Benzyloxycarbonyl)-1-(4-methoxyphenylsulfonyl)-N-hydroxypiperazine-2-carboxamide
benzyl 3-(hydroxycarbamoyl)-4-(4-methoxyphenyl)sulfonylpiperazine-1-carboxylate
PD039849
MMP-9/MMP-13 Inhibitor ll CalBioChem Cat. No. 444253
3-Hydroxycarbamoyl-4-(4-methoxy-benzenesulfonyl)-piperazine-1-carboxylic acid benzyl ester