Skip to main content

Chloramine-T

ADVERTISEMENT
Identification
Molecular formula
C7H7Cl2N2O2S
CAS number
127-65-1
IUPAC name
2,4-dichloro-1-[[methyl(sulfamoyl)amino]methyl]benzene
State
State

At room temperature, Chloramine-T is typically a solid.

Melting point (Celsius)
167.00
Melting point (Kelvin)
440.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
281.64g/mol
Molar mass
281.6390g/mol
Density
1.5000g/cm3
Appearence

Chloramine-T typically appears as white crystals or a white crystalline powder.

Comment on solubility

Solubility of 2,4-Dichloro-1-[[methyl(sulfamoyl)amino]methyl]benzene

The compound 2,4-dichloro-1-[[methyl(sulfamoyl)amino]methyl]benzene exhibits distinct solubility characteristics, influenced by its chemical structure and functional groups.

Key insights into its solubility:

  • Polarity: The presence of both a chloro and a sulfamoyl group contributes to a degree of polarity, which affects its solubility in various solvents.
  • Solvent compatibility: This compound is likely to be more soluble in polar solvents such as water and methanol, while showing decreased solubility in nonpolar solvents like hexane.
  • Hydrogen bonding: The sulfamoyl group introduces potential for hydrogen bonding, which may enhance solubility in aqueous solutions.

In conclusion, understanding the solubility behavior of 2,4-dichloro-1-[[methyl(sulfamoyl)amino]methyl]benzene can be essential for applications in various chemical processes. As with many compounds, the interplay of functional groups and molecular structure plays a critical role in determining its solubility profile.

Interesting facts

Interesting Facts about 2,4-Dichloro-1-[[methyl(sulfamoyl)amino]methyl]benzene

2,4-Dichloro-1-[[methyl(sulfamoyl)amino]methyl]benzene is a fascinating compound that holds significance in various chemical and pharmaceutical contexts. Here are some intriguing facts about this compound:

  • Pharmaceutical Relevance: This compound has been studied for its potential application as a pharmaceutical agent, particularly in the realm of antibacterial and anti-inflammatory treatments.
  • Sulfamoyl Group: The presence of the sulfamoyl functional group is particularly noteworthy, as it can enhance the biological activity of the compound due to its ability to mimic naturally occurring sulfonamide antibiotics.
  • Chlorine Atoms: The two chlorine atoms attached to the benzene ring can affect the compound's reactivity and how it interacts with biological systems, often increasing lipophilicity – a key factor in drug design.
  • Structure-Activity Relationship: This compound is a prime example for studies on structure-activity relationships (SAR), enabling researchers to modify the structure and evaluate the changes in activity and efficacy.
  • Basic Chemistry: Understanding the chemistry behind compound formation, including substitution reactions, is essential, as it showcases the interplay of various functional groups in organic synthesis.
  • Environmental Considerations: Researchers also pay attention to the environmental impact of dichlorinated compounds, assessing their stability and degradation pathways in ecological studies.

This compound exemplifies the complexity and beauty of synthetic chemistry while opening doors to potential medicinal applications. As a student or scientist, delving into its properties can uncover new insights and applications in both chemistry and medicine.

Synonyms
SAH 1462
4960-47-8
Sulfamide, N-(2,4-dichlorobenzyl)-N-methyl-
BRN 2943163
N-METHYL-N-(2,4-DICHLOROBENZYL)SULFAMIDE
DTXSID80197927
DTXCID40120418
2,4-dichloro-1-[[methyl(sulfamoyl)amino]methyl]benzene