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No common scientific name

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Identification
Molecular formula
C15H13NO7
CAS number
554-03-6
IUPAC name
amino 5-[(3-aminooxycarbonyl-4-hydroxy-phenyl)-(3-aminooxycarbonyl-4-oxo-cyclohexa-2,5-dien-1-ylidene)methyl]-2-hydroxy-benzoate
State
State

At room temperature, it exists as a dark red solid.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
285.24g/mol
Molar mass
285.2350g/mol
Density
1.4600g/cm3
Appearence

The compound is a dark red solid.

Comment on solubility

Solubility of Amino 5-[(3-aminooxycarbonyl-4-hydroxy-phenyl)-(3-aminooxycarbonyl-4-oxo-cyclohexa-2,5-dien-1-ylidene)methyl]-2-hydroxy-benzoate

The compound with the chemical formula C15H13NO7 presents intriguing solubility characteristics, influenced by its complex structure and functional groups. Solubility is pivotal in determining the behavior of compounds, particularly in biological systems and chemical reactions.

General Solubility Information

This particular compound is expected to exhibit varying degrees of solubility depending on the solvent employed. Factors that often influence the solubility of such compounds include:

  • Polarity of the Solvent: The presence of polar functional groups, such as hydroxyls and amines, suggests that this compound may be more soluble in polar solvents like water.
  • Hydrogen Bonding: The capability to form hydrogen bonds can enhance solubility in polar solvents. This compound's hydroxyl and amino groups facilitate such interactions.
  • Size and Steric Hindrance: The larger, more complex structure can sometimes lead to decreased solubility due to steric hindrance and reduced interactions with solvent molecules.

Expected Solubility Behavior

While specific solubility data for this compound is not readily available, one might infer that:

  • The compound may be moderately soluble in water due to its polar groups.
  • It might have better solubility in organic solvents that can interact favorably with its non-polar segments.
  • The solubility may alter with pH, particularly given the presence of acidic and basic functional groups.

Understanding the solubility behavior of this compound is crucial for applications in pharmaceuticals, materials science, and environmental studies. As the solubility directly impacts the bioavailability and efficacy of compounds, further experimental verification would be essential in exploring its potential uses.

Interesting facts

Interesting Facts about Amino 5-[(3-aminooxycarbonyl-4-hydroxy-phenyl)-(3-aminooxycarbonyl-4-oxo-cyclohexa-2,5-dien-1-ylidene)methyl]-2-hydroxy-benzoate

This compound, with its complex structure, is a fascinating example of how functional groups can interact, leading to diverse biological activities. It belongs to the class of amino acids and is notably recognized for its potential medicinal applications, particularly in the field of drug design.

Key Features:

  • Bioactivity: The compound is known for its intriguing biological properties, which may include anti-inflammatory and antioxidant effects, making it a subject of interest in pharmaceutical research.
  • Structure Diversity: Its unique structure incorporates multiple active sites, allowing it to participate in various biochemical interactions, enhancing its potential utility in targeted therapies.
  • Derivatives and Synthesis: The synthesis of this compound can be quite challenging due to its intricate multi-step procedures. Researchers often explore derivatives of this molecule to enhance effectiveness or reduce side effects.

As a testimony of its complexity, scientists often remark, “A compound that appears simple can be a treasure trove of surprises!” This highlights the potential for new discoveries that can stem from compounds with elaborate chemical frameworks.

Applications in Research:

  • Drug Development: The structure can serve as a lead compound in the exploration of new drugs.
  • Study of Enzymatic Interactions: Its distinct functionalities may impact enzyme activity, allowing researchers to explore new biochemical pathways.

The exploration of Amino 5-[(3-aminooxycarbonyl-4-hydroxy-phenyl)-(3-aminooxycarbonyl-4-oxo-cyclohexa-2,5-dien-1-ylidene)methyl]-2-hydroxy-benzoate opens up numerous avenues for scientific inquiry, emphasizing the intersection of chemistry and biology in developing innovative therapeutic strategies.

Synonyms
TG2-222-5
cid_2258
CHEMBL1569779
BDBM41963
SMP2_000091
amino 5-[(3-aminooxycarbonyl-4-hydroxyphenyl)-(3-aminooxycarbonyl-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]-2-hydroxybenzoate
5-[(3-aminooxycarbonyl-4-hydroxy-phenyl)-(3-aminooxycarbonyl-4-keto-cyclohexa-2,5-dien-1-ylidene)methyl]-2-hydroxy-benzoic acid amino ester
5-[[3-[aminooxy(oxo)methyl]-4-hydroxyphenyl]-[3-[aminooxy(oxo)methyl]-4-oxo-1-cyclohexa-2,5-dienylidene]methyl]-2-hydroxybenzoic acid amino ester
azanyl 5-[(3-azanyloxycarbonyl-4-oxidanylidene-cyclohexa-2,5-dien-1-ylidene)-(3-azanyloxycarbonyl-4-oxidanyl-phenyl)methyl]-2-oxidanyl-benzoate