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BAM Br (5-Amino-1,2,4-dithiazol-3-ylidene)ammonium bromide

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Identification
Molecular formula
C2H5N4S2Br
CAS number
57863-61-7
IUPAC name
(5-amino-1,2,4-dithiazol-3-ylidene)ammonium;bromide
State
State

At room temperature, (5-amino-1,2,4-dithiazol-3-ylidene)ammonium; bromide is typically a solid.

Melting point (Celsius)
185.00
Melting point (Kelvin)
458.15
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
256.11g/mol
Molar mass
256.1100g/mol
Density
2.2200g/cm3
Appearence

The compound appears as a yellow crystalline solid. It may form fine needles or powder and is generally stable under standard conditions. The unique thiazole ring structure may contribute to its distinct bright yellow coloration.

Comment on solubility

Solubility of (5-amino-1,2,4-dithiazol-3-ylidene)ammonium bromide

The solubility of (5-amino-1,2,4-dithiazol-3-ylidene)ammonium bromide can be characterized by several important factors that contribute to its behavior in various solvents.

Key Points on Solubility:

  • Polarity: Due to the presence of the ammonium ion and the bromide anion, this compound is likely to exhibit high solubility in polar solvents, particularly water.
  • Hydrogen Bonding: The amino group in the compound may engage in hydrogen bonding interactions, enhancing its solubility in aqueous solutions.
  • Temperature Dependency: The solubility may increase with temperature, a common trait for many ionic compounds, allowing more of the substance to dissolve in warm solutions.
  • pH Influence: Changes in pH can affect solubility; at higher pH levels, the amino group may be more protonated, potentially altering its solubility profile.

In general, it is important to note that while the compound is expected to be soluble in water, solubility can vary based on concentration and temperature. For specific applications, further empirical data on solubility is recommended, as individual behaviors can differ based on environmental factors.

Interesting facts

Interesting Facts about (5-amino-1,2,4-dithiazol-3-ylidene)ammonium; bromide

(5-amino-1,2,4-dithiazol-3-ylidene)ammonium; bromide is a fascinating compound that demonstrates the intriguing properties of nitrogen and sulfur chemistry. Here are some notable facts:

  • Biological Relevance: Compounds containing the dithiazole moiety are often studied for their potential biological activities, including antimicrobial and antifungal properties.
  • Coordination Chemistry: The presence of nitrogen in its structure allows this compound to act as a ligand, forming coordination complexes with various metals, broadening its application in material science and catalysis.
  • Research Applications: This compound may find use in synthetic organic chemistry, especially when researching new synthetic pathways or creating novel materials with unique electronic properties.
  • Structure and Stability: The ylidene functionality in the compound contributes to its stability and reactivity, making it an interesting subject in the study of reactive intermediates.
  • Potential Uses: Its unique chemical characteristics open avenues for use in designing new drugs or materials, particularly in the fields of chemistry and pharmacology.
  • Historical Context: Dithiazoles have been a part of chemical research since the mid-20th century, playing significant roles in the development of various chemical industries.

In summary, the unique qualities of (5-amino-1,2,4-dithiazol-3-ylidene)ammonium; bromide make it an appealing subject for ongoing research, especially in the realms of pharmacology and material science. As with many specialized compounds, understanding its behavior could lead to innovative applications that may significantly impact various technological fields.

Synonyms
1,2,4-DITHIAZOL-1-IUM, 3,5-DIAMINO-, BROMIDE
7364-95-6