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N1-Allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide

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Identification
Molecular formula
C13H15ClN2O5S2
IUPAC name
N1-allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide
State
State

At room temperature, it is generally expected to be a solid due to its complex structure and the presence of multiple functional groups which contribute to intermolecular interactions.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
368.85g/mol
Molar mass
0.0000g/mol
Density
0.0000g/cm3
Appearence

N1-Allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide typically appears as a solid compound at room temperature. The specific appearance, such as color or crystalline form, would typically need to be determined from empirical observations or experimental data, which are not available in common databases.

Comment on solubility

Solubility of N1-allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide

The solubility characteristics of N1-allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide can be intriguing due to its complex structure. Understanding its solubility can help predict its behavior in various environments, including biological systems.

Factors Influencing Solubility:

  • Polarity: The presence of sulfonamide groups increases the polarity, generally enhancing solubility in polar solvents.
  • Solvent Interaction: This compound may have variable solubility in organic solvents like ethanol and methanol compared to water due to its potential functional groups.
  • Temperature: Like many chemical compounds, solubility can increase with temperature; thus, heating may enhance its dissolving potential.

It is essential to note that the solubility can vary widely based on specific factors. In summary, "the solubility of N1-allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide is influenced by its structural properties, polarity, and environmental conditions." This complexity underscores the importance of conducting experimental solubility tests for precise applications in scientific research.

Interesting facts

Interesting Facts About N1-allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide

This remarkable compound, known for its unique structure and potential applications, showcases the beauty of organic chemistry in the realm of medicinal compounds. Here are some intriguing points about N1-allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide:

  • Inhibition Potential: Compounds like this often serve as inhibitors in various biological pathways, making them valuable in the development of new drugs.
  • Functional Groups: The presence of sulfonamide groups greatly enhances the physiological activity, allowing for a diversity of interactions with biological targets.
  • Design Versatility: The structural characteristics provide opportunities for modifying the compound to optimize its pharmacological properties, including bioavailability and selectivity.
  • Research Applications: Scientists are actively exploring such compounds for their use in cancer therapy, where the inhibition of specific enzymes can slow down tumor growth.
  • Synthetic Chemistry: The synthesis of this compound involves intricate organic reactions, which can be a great learning experience for students interested in developing their synthetic skills.

In summary, N1-allyl-4-chloro-6-(3-oxobut-1-enylamino)benzene-1,3-disulfonamide exemplifies the success of chemical modifications that aim to enhance biological activity. Its compelling nature continues to inspire chemists and researchers alike to unlock its full therapeutic potential.

Synonyms
AMBUSIDE
3754-19-6
Ambusida
EX 4810
VCM261MOO0
RMI 83,047
1,3-Benzenedisulfonamide, 4-chloro-6-((3-hydroxy-2-butenylidene)amino)-N(sup 1)-2-propenyl-
N(sup 1)-Allyl-4-chloro-6-((3-hydroxy-2-butenylidene)amino)-m-benzenedisulfonamide
Ambusidum
RMI-83047
EX-4810
EX 4810; Hydrion; Novohydrin; RMI 83047
AMBUSIDE [USAN]
Ambusidum [INN-Latin]
AMBUSIDE [INN]
AMBUSIDE [MI]
Ambusida [INN-Spanish]
AMBUSIDE [MART.]
UNII-VCM261MOO0
Ambuside [USAN:INN:BAN]
DTXSID60877210
EINECS 223-158-4
RMI 83047
RC 4810
NS00045801
Q27291757
1,3-Benzenedisulfonamide, 4-chloro-6-((3-hydroxy-2-butenylidene)amino)-N1-2-propenyl-
4-chloro-6-(3-oxobut-1-enylamino)-1-N-prop-2-enylbenzene-1,3-disulfonamide
5-ALLYLSULFAMOYL-2-CHLORO-4-(3-HYDROXYBUT-2-ENYLIDENEAMINO)BENZENESULFONAMIDE
N'-ALLYL-4-CHLORO-6-((3-HYDROXY-2-BUTENYLIDENE)AMINO)-M-BENZENEDISULFONAMIDE
N1-Allyl-4-chlor-6-((3-hydroxy-2-butenyliden)amino)-1,3-benzoldisulfonamid
N1-Allyl-4-chloro-6-((3-hydroxy-2-butenylidene)amino)-m-benzenedisulfonamide