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S-(2-aminoethyl) benzenecarbothioate

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Identification
Molecular formula
C9H11NS
CAS number
52663-82-4
IUPAC name
S-(2-aminoethyl) benzenecarbothioate
State
State

At room temperature, S-(2-aminoethyl) benzenecarbothioate is found in a liquid state. It maintains this state under standard laboratory conditions.

Melting point (Celsius)
-4.00
Melting point (Kelvin)
269.20
Boiling point (Celsius)
280.50
Boiling point (Kelvin)
553.70
General information
Molecular weight
183.26g/mol
Molar mass
183.2610g/mol
Density
1.1000g/cm3
Appearence

The compound S-(2-aminoethyl) benzenecarbothioate typically appears as a pale yellow to yellow liquid. It may also be observed as a viscous liquid depending on the specific formulation or sample concentration.

Comment on solubility

Solubility of S-(2-aminoethyl) benzenecarbothioate

S-(2-aminoethyl) benzenecarbothioate is an intriguing compound whose solubility characteristics can be described through a few notable aspects:

  • Polarity: The presence of an amino group in its structure generally lends some degree of polarity to the compound. This can affect its solubility in both water and organic solvents.
  • Hydrogen Bonding: The amino group can engage in hydrogen bonding, which may enhance its solubility in polar solvents, such as water.
  • Solvent Compatibility: Hexane or other non-polar solvents might not solvate the compound well due to its polar characteristics. Therefore, you may find better solubility in solvents like ethanol or methanol.
  • Temperature Influence: Temperature also plays a critical role—generally, increasing the temperature can improve the solubility of organic compounds in liquids.

In summary, while the specific solubility parameters of S-(2-aminoethyl) benzenecarbothioate may vary, its ability to dissolve in polar solvents makes it a compound of interest in various applications. As with many chemical species, understanding its solubility is key to leveraging its full potential in chemical processes.

Interesting facts

Interesting Facts about S-(2-aminoethyl) benzenecarbothioate

S-(2-aminoethyl) benzenecarbothioate is a fascinating compound that belongs to the thioester family, known for their unique bonding and reactivity. This compound exhibits a variety of chemical properties and potential applications that are of particular interest in the field of organic chemistry.

Key Characteristics

  • Biological Relevance: Compounds similar to S-(2-aminoethyl) benzenecarbothioate are often studied for their roles in biological systems, particularly as metabolic intermediates.
  • Synthesis: The synthesis of this compound typically involves thioesterification reactions, providing an excellent example of how diverse functional groups can be created in organic synthesis.
  • Potential Applications: Due to its structure, this compound may serve as a precursor in the manufacture of various pharmaceuticals or agrochemicals, making it relevant for both medicinal and agricultural chemistry.

Chemical Reactivity

The thioester functional group makes S-(2-aminoethyl) benzenecarbothioate highly reactive. Here are some reactions that may occur:

  • Nucleophilic Attack: The sulfur atom can undergo nucleophilic substitution reactions, facilitating further modifications.
  • Hydrolysis: This compound can be hydrolyzed to release the corresponding carboxylic acid and a thiol, which is a reaction of substantial interest in biochemical pathways.

Notable Studies

Research exploring various thioester compounds, including S-(2-aminoethyl) benzenecarbothioate, often highlights their importance in enzyme catalysis and metabolic processes. Scientists are captivated by how these compounds can act as substrates for enzymes, leading to transformations that are crucial for life.

In conclusion, S-(2-aminoethyl) benzenecarbothioate exemplifies the broad and intricate world of organic compounds, underscoring the importance of thioesters in both chemistry and biochemistry. Its diverse applications and reactivity offer endless opportunities for exploration and discovery.

Synonyms
S-BENZOYLCYSTEAMINE
46053-57-0
654-942-8
S-(2-Aminoethyl) benzothioate
SCHEMBL6549496
AKOS006274421