Skip to main content

2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium dibromide

ADVERTISEMENT
Identification
Molecular formula
C9H13Br2N3S
CAS number
.
IUPAC name
2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium;dibromide
State
State

At room temperature, 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium dibromide is typically found in a solid state, often as a crystalline or powdery substance.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
335.10g/mol
Molar mass
335.1580g/mol
Density
1.7000g/cm3
Appearence

This compound typically presents as a crystalline solid that may appear as white or off-white in color. The detailed crystalline structure can be better understood through techniques such as X-ray crystallography, revealing molecular arrangements.

Comment on solubility

Solubility of 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium;dibromide

The solubility of the compound 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium;dibromide can be understood through several key factors. This compound contains multiple functional groups that influence its interaction with various solvents:

  • Nature of the Compound: Being a quaternary ammonium derivative suggests that it has a polar character which generally favors solubility in polar solvents like water.
  • Ionic Nature: The presence of dibromide indicates that this compound is likely to form ionic interactions, enhancing solubility in water by dissociating into ions.
  • Hydrogen Bonding: The amine and sulfur functionalities present can participate in hydrogen bonding, which may improve solubility further in polar environments.

In summary, one can expect 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium;dibromide to exhibit good solubility in polar solvents, particularly water, due to its ionic characteristics and polar functional groups. However, solubility may be reduced in nonpolar solvents due to its overall structure. It's important to experiment with specific solvent systems to determine the precise solubility behavior.

Interesting facts

Interesting Facts about 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium Dibromide

2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium dibromide is a fascinating compound that has captured the interest of scientists due to its unique properties and potential applications. Here are some noteworthy facts:

  • Biological Significance: This compound is associated with various biological activities, particularly in the field of medicinal chemistry. Compounds containing benzimidazole moieties are known to exhibit antibacterial, antifungal, and anticancer properties.
  • Synthesis and Reactivity: The synthesis of this compound involves specific reactions that showcase the ability to modify its structure for enhanced efficacy. The introduction of the benzimidazolium group significantly influences its reactivity.
  • Cationic Nature: Being a quaternary ammonium compound, it carries a positive charge, which enhances its interaction with negatively charged biological membranes, making it a subject of study in drug delivery systems.
  • Versatile Applications: Researchers are exploring its use in various fields, including:
    • Pharmaceutical formulations
    • Biological imaging
    • Therapeutic agents for various diseases
  • Structure-Activity Relationship (SAR): The relationship between the structure of benzimidazolium compounds and their biological activity is an active area of research, with many scientists working towards deciphering how structural modifications can lead to improved therapeutic effects.

In conclusion, 2-(1H-benzimidazol-3-ium-2-ylsulfanyl)ethylammonium dibromide represents a significant intersection of organic chemistry and medicinal science. Its unique properties warrant further investigation, which could lead to advancements in treatment options for infectious diseases and cancer.

Synonyms
2-(2-Aminoethylmercapto)benzimidazoline bromide hydrobromide
BENZIMIDAZOLE, 2-((2-AMINOETHYL)THIO)-, DIHYDROBROMIDE
2-((2-Aminoethyl)thio)benzimidazole dihydrobromide
7673-88-3