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DDBN

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Identification
Molecular formula
C14H21N3O3
CAS number
5001-18-3
IUPAC name
4-(dimethylamino)-N-[5-(hydroxyamino)-5-oxo-pentyl]benzamide
State
State

At room temperature, DDBN is typically found in solid form.

Melting point (Celsius)
189.00
Melting point (Kelvin)
462.15
Boiling point (Celsius)
524.00
Boiling point (Kelvin)
797.15
General information
Molecular weight
279.36g/mol
Molar mass
279.3550g/mol
Density
1.2370g/cm3
Appearence

DDBN appears as a white crystalline compound.

Comment on solubility

Solubility of 4-(dimethylamino)-N-[5-(hydroxyamino)-5-oxo-pentyl]benzamide

The solubility of 4-(dimethylamino)-N-[5-(hydroxyamino)-5-oxo-pentyl]benzamide (C14H21N3O3) can be influenced by various factors related to its chemical structure and functional groups. To explore its solubility characteristics, consider the following points:

  • Polarity: The presence of amino and hydroxyl groups generally increases the polarity of the compound, potentially enhancing its solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability of hydroxyamino and amide groups to form hydrogen bonds can significantly promote solubility in aqueous environments.
  • Carbon Chain Length: The long alkyl chain may introduce hydrophobic characteristics which can limit solubility in polar solvents but may enhance solubility in organic solvents.
  • pH Sensitivity: The solubility can also be affected by pH levels due to the ionization of amino groups, making it more soluble under certain acidic or basic conditions.

In summary, the solubility of this compound is likely a balance between its polar functionalities that favor solubility in water and its hydrophobic alkyl group that may restrict solubility in polar media. Testing in multiple solvents will provide a clearer understanding of its solubility profile.

Interesting facts

Interesting Facts about 4-(Dimethylamino)-N-[5-(hydroxyamino)-5-oxo-pentyl]benzamide

This chemical compound, known for its complex structure and fascinating properties, plays an intriguing role in various fields of chemistry and biotechnology. Below are some key points highlighting its significance:

  • Pharmaceutical Relevance: Many compounds of this class are investigated for their potential therapeutic effects, particularly in the realm of cancer research and drug design.
  • Amine Functionality: The presence of the −N(dimethyl) group suggests interesting interactions with biological systems, potentially enhancing the bioavailability and efficacy of related pharmaceutical candidates.
  • Hydroxyamino Group: The −OH and −NH2 moieties can participate in hydrogen bonding, which may influence the compound's solubility and reactivity, making it a point of interest in studying ligand binding to various targets.
  • Structure-Activity Relationship (SAR): Compounds with similar structures are often analyzed in SAR studies, providing insights into how modifications to the molecular framework can enhance desired properties or reduce side effects.

As a science enthusiast or a chemistry student, one can appreciate how the intricate balance of electron-donating and electron-withdrawing groups in this compound can lead to varied chemical reactivity and biological activity. Understanding such compounds is crucial for developing effective therapeutic agents and advancing medicinal chemistry.

“Chemistry is the art of understanding how and why things interact at the molecular level.” This compound perfectly embodies that essence, offering a wealth of opportunities for exploration and discovery in the ever-evolving field of chemistry.

Synonyms
CHEMBL142305
4-(dimethylamino)-N-[5-(hydroxyamino)-5-oxopentyl]benzamide
251456-58-3
HDInhib_000015
SCHEMBL13039726
DTXSID90274410
BDBM50082662
4-Dimethylamino-N-(4-hydroxycarbamoyl-butyl)-benzamide