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2-Mercaptoacetamidine

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Identification
Molecular formula
C2H6N2S
CAS number
593-84-0
IUPAC name
2-sulfanylacetamidine
State
State

At room temperature, 2-mercaptoacetamidine exists as a solid. It is known for being stable under normal conditions, though it should be handled with care due to its potential irritant properties.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
238.00
Boiling point (Kelvin)
511.15
General information
Molecular weight
90.15g/mol
Molar mass
90.1530g/mol
Density
1.1360g/cm3
Appearence

2-Mercaptoacetamidine appears as a colorless to pale yellow crystalline solid. It is often characterized by its slight sulfur odor.

Comment on solubility

Solubility of 2-sulfanylacetamidine

2-sulfanylacetamidine, with the chemical formula C3H8N2S, displays intriguing solubility properties that can be influenced by various factors:

  • Polarity: This compound contains both polar and non-polar functional groups. The presence of the thiol (-SH) group contributes to its polar characteristics, which may enhance solubility in polar solvents such as water.
  • Hydrogen bonding: Due to the amine functional group, 2-sulfanylacetamidine can engage in hydrogen bonding, which significantly increases its solubility in water and other polar solvents.
  • pH dependency: The solubility of 2-sulfanylacetamidine may vary with pH changes, as protonation of the amine group can influence the ionic character of the compound.
  • Solvent compatibility: While 2-sulfanylacetamidine is likely soluble in aqueous solutions, it may exhibit varying solubility in organic solvents, depending on their polarities.

In summary, the solubility of 2-sulfanylacetamidine can be characterized by its potential to dissolve in polar solvents, where factors such as polarity, hydrogen bonding, pH, and solvent compatibility play crucial roles. Understanding these aspects provides valuable insight into the compound's behavior in different environments.

Interesting facts

Interesting Facts About 2-Sulfanylacetamidine

2-Sulfanylacetamidine is a fascinating compound that belongs to the category of sulfur-containing organic molecules. Here are some intriguing aspects of this compound:

  • Biological Significance: Compounds like 2-sulfanylacetamidine are often studied for their biological properties, particularly their potential roles as pharmaceuticals or agrochemicals.
  • Chemical Properties: The presence of the sulfanyl group introduces unique reactivity patterns, making it interesting for organic synthesis. It can act as a nucleophile, participating in various chemical reactions.
  • Potential Applications: Researchers are investigating 2-sulfanylacetamidine for its potential applications in developing antiviral and anticancer agents. Compounds that modify biological pathways are vital in medicinal chemistry.
  • Structural Motivation: The distinct structure of 2-sulfanylacetamidine, featuring both sulfur and nitrogen atoms, allows it to adopt interesting conformations that can influence its reactivity and interaction with biological targets.
  • Functional Group Chemistry: Understanding how the sulfanyl functional group interacts with other functional groups in organic synthesis helps chemists design new compounds with desired characteristics. This highlights the versatility of sulfur in organic chemistry.

In summary, 2-sulfanylacetamidine showcases the intricate relationship between chemical structure and function, and it opens up avenues for research that could lead to groundbreaking discoveries in medicinal chemistry and related fields. As stated by renowned chemist Marie Curie, "Nothing in life is to be feared, it is only to be understood." The study of such compounds embodies this pursuit of understanding in the realm of science.

Synonyms
50433-21-1
Ethanimidamide, 2-mercapto-
DTXSID30274878
DTXCID70226331
RefChem:340594
2-sulfanylethanimidamide
Mercaptoacetamidine
SCHEMBL1551312
CHEMBL3304035
SCHEMBL10384512
AKOS006362270
EN300-199507