Skip to main content

Thioglycolylglycine

ADVERTISEMENT
Identification
Molecular formula
C4H7NO3S
CAS number
929-53-9
IUPAC name
2-(2-amino-2-oxo-ethyl)sulfanylacetamide
State
State

At room temperature, Thioglycolylglycine is in a solid state.

Melting point (Celsius)
143.00
Melting point (Kelvin)
416.15
Boiling point (Celsius)
232.00
Boiling point (Kelvin)
505.15
General information
Molecular weight
149.19g/mol
Molar mass
149.1850g/mol
Density
1.4450g/cm3
Appearence

Thioglycolylglycine typically appears as a crystalline solid with a color ranging from white to off-white. It is a relatively stable solid under standard conditions.

Comment on solubility

Solubility of 2-(2-amino-2-oxo-ethyl)sulfanylacetamide

The solubility of 2-(2-amino-2-oxo-ethyl)sulfanylacetamide can be influenced by various factors including temperature, pH, and the presence of other solvents. This compound, known for its unique structural properties, generally exhibits moderate solubility in polar solvents such as water and methanol. Here are some key points concerning its solubility:

  • Polarity: The nitrogen and sulfur functional groups promote interactions with polar solvents, facilitating solubility.
  • Temperature Dependence: Increasing temperature typically enhances solubility, allowing for greater dissolution rates.
  • pH Influence: The ionizable amine group can affect solubility based on pH levels; for instance, under acidic conditions, the compound may become more soluble.
  • Hydrogen Bonding: The presence of amino and oxo groups enhances potential hydrogen bonding with solvent molecules, aiding in solubility.

In summary, 2-(2-amino-2-oxo-ethyl)sulfanylacetamide exhibits favorable solubility characteristics in polar environments, but may require specific conditions to optimize its dissolution in various applications. Understanding these factors is essential for using this compound effectively in chemical processes.

Interesting facts

Interesting Facts about 2-(2-amino-2-oxo-ethyl)sulfanylacetamide

2-(2-amino-2-oxo-ethyl)sulfanylacetamide, often referred to as a derivative in the realm of organic compounds, exhibits fascinating characteristics that make it an intriguing subject for both chemists and students alike. Here are some notable points:

  • Biological Relevance: This compound plays a role in biological systems, potentially serving as a precursor to important biochemical pathways, which may contribute to therapeutic activities.
  • Functional Group Diversity: The presence of multiple functional groups, such as the amine, carbonyl, and sulfanyl groups, offers insight into various chemical reactivity patterns, expanding the potential applications in medicinal chemistry.
  • Synthesis Versatility: Synthetic pathways to create this compound often involve innovative reactions, showcasing the versatility of organic synthesis techniques, which can serve as a learning experience for aspiring chemists.
  • Analytical Techniques: Characterization of this compound often requires the use of sophisticated analytical methods such as NMR spectroscopy and mass spectrometry, which help in understanding its structure and properties better.
  • Potential Applications: Given its structural complexity, it holds promise for various applications in pharmaceuticals, including potential roles as a drug candidate or a biochemical probe.

In summary, 2-(2-amino-2-oxo-ethyl)sulfanylacetamide stands out not only for its chemical properties but also for its implications in real-world chemistry. As chemistry continues to evolve, compounds like this one remind us of the intricate relationships between molecular structure and function.

Synonyms
14618-65-6
2,2'-Thiobisacetamide
Thiodiglycolamide
Thiodiacetamide
Thiobisacetamide
ACETAMIDE, 2,2'-THIOBIS-
2,2'-Thio-bis-acetamide
EINECS 238-657-2
G4Y5Q1UXX2
NSC 82327
BRN 1764428
MEXORYL SA
NSC-82327
DTXSID30163293
4-03-00-00625 (Beilstein Handbook Reference)
THIODIGLYCOLAMIDE [INCI]
DTXCID1085784
2,2'-Thiodiacetamide
2-(2-amino-2-oxoethyl)sulfanylacetamide
CHEMBL171496
2,2/'-THIODIACETAMIDE
2-Carbamoylmethylsulfanyl-acetamide
2-(carbamoylmethylthio)acetamide
UNII-G4Y5Q1UXX2
monothiodiacetamide
NSC82327
Acetamide,2'-thiobis-
2,2'-Thiobis(acetamide)
WLN: ZV1S1VZ
SCHEMBL3069757
SCHEMBL5841715
BDBM50224826
SBB058334
AKOS003325212
2-(2-amino-2-oxo-ethyl)sulfanylacetamide
DB-042829
CS-0337195
NS00014154
ST45023917
Q27278754