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N-Bromoethyl-N-chloro-isoindoline-sulfonamide

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Identification
Molecular formula
C10H8BrClNO4S
CAS number
883915-02-2
IUPAC name
2-(2-bromoethyl)-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide
State
State

The compound is in solid state at room temperature, characterizing it as a stable compound under standard conditions, suited for various chemical applications that require halogenated sulfonamide derivates.

Melting point (Celsius)
220.50
Melting point (Kelvin)
493.65
Boiling point (Celsius)
485.20
Boiling point (Kelvin)
758.35
General information
Molecular weight
365.56g/mol
Molar mass
365.5630g/mol
Density
2.0201g/cm3
Appearence

The compound appears as a crystalline solid, typically with a light yellow to off-white coloration. Being a derivative containing halogen and sulfonamide groups, its solid form can exhibit a slightly granular texture, characteristic of many aromatic organic compounds.

Comment on solubility

Solubility of 2-(2-bromoethyl)-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide

The solubility of 2-(2-bromoethyl)-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide is an interesting aspect due to its structural complexity and functional groups. Here are some significant points regarding its solubility characteristics:

  • Polarity: The presence of sulfonamide and dioxo groups suggests that this compound is likely to be polar, which can enhance its solubility in polar solvents.
  • Solvents: It may exhibit improved solubility in solvents such as water and alcohols due to hydrogen bonding capability.
  • Temperature Effects: As with many compounds, its solubility may increase with temperature; thus, heating the solvent could be beneficial for dissolution.
  • pH Dependence: The solubility could vary with the pH of the solution, particularly due to the sulfonamide group, which can interact differently under acidic or basic conditions.

In summary, while specific solubility data may vary globally, understanding the interactions and chemical nature of this compound allows us to predict that 2-(2-bromoethyl)-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide might be moderately soluble in polar solvents, especially when conditions like temperature and pH are optimized.

Interesting facts

Interesting Facts about 2-(2-bromoethyl)-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide

This compound is a fascinating member of the isoindoline family, exhibiting a unique structure that combines multiple functional groups contributing to its chemical properties and potential applications. Here are some intriguing aspects of 2-(2-bromoethyl)-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide:

  • Diverse Functional Groups: The presence of a sulfonamide group in this compound is particularly notable, as sulfonamides are known for their biological activity, including antimicrobial properties.
  • Halogen Substitution: The inclusion of both a bromo and chloro substituent suggests potential reactivity in various organic transformations, making this compound a valuable intermediate in synthetic chemistry.
  • Potential Applications: Due to its intriguing structure, this compound may find use in medicinal chemistry, especially in the development of new pharmacological agents.
  • Isoindoline Chemistry: Isoindoline derivatives have attracted considerable attention in research due to their applications in dye manufacturing and as precursors for organic light-emitting diodes (OLEDs).
  • Synergistic Effects: The combination of the sulfonamide functionality and the unique heterocyclic framework may result in enhanced biological activities or novel effects, warranting further investigation.

In summary, 2-(2-bromoethyl)-6-chloro-1,3-dioxo-isoindoline-5-sulfonamide represents a compelling example of how organic chemistry can yield compounds with significant potential for innovation in both pharmaceuticals and materials science. As “the most successful innovations often arise from unexpected combinations”, this compound embodies the spirit of exploration and discovery in the chemical sciences.

Synonyms
BRN 0432853
5-ISOINDOLINESULFONAMIDE, 2-(2-BROMOETHYL)-6-CHLORO-1,3-DIOXO-
3822-97-7
2-(2-Bromoethyl)-6-chloro-1,3-dioxo-5-isoindolinesulfonamide
5-22-07-00596 (Beilstein Handbook Reference)
1H-Isoindole-5-sulfonamide, 2-(2-bromoethyl)-6-chloro-2,3-dihydro-1,3-dioxo-
DTXSID50191598
DTXCID90114089