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S-Alkylcysteine

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Identification
Molecular formula
C5H10ClNO2S
CAS number
82419-36-1
IUPAC name
2-amino-3-(2-chloroethylsulfanyl)propanoic acid
State
State

S-Alkylcysteine is typically solid at room temperature.

Melting point (Celsius)
234.00
Melting point (Kelvin)
507.20
Boiling point (Celsius)
205.40
Boiling point (Kelvin)
478.60
General information
Molecular weight
183.67g/mol
Molar mass
183.6650g/mol
Density
1.5360g/cm3
Appearence

S-Alkylcysteine typically appears as a white crystalline solid.

Comment on solubility

Solubility of 2-amino-3-(2-chloroethylsulfanyl)propanoic acid

The solubility of 2-amino-3-(2-chloroethylsulfanyl)propanoic acid in various solvents highlights its unique chemical structure and potential applications. Here are some key points to consider:

  • Water Solubility: This compound is expected to be significantly soluble in water due to the presence of both an amino group and a carboxylic acid group, which can form hydrogen bonds and polar interactions with water molecules.
  • Solvent Variability: While it shows good solubility in polar solvents such as methanol and ethanol, its solubility in non-polar solvents like hexane will be limited.
  • Temperature Dependence: The solubility might increase with temperature, a common phenomenon for many organic acids, due to enhanced molecular motion which facilitates dissolution.
  • pH Influence: The pH of the solution can play a significant role; at low pH levels, the carboxylic acid group can remain protonated, affecting its overall solubility characteristics.

In summary, the solubility profile of 2-amino-3-(2-chloroethylsulfanyl)propanoic acid is predominantly influenced by its polar functional groups, making it amenable to interaction with aqueous environments while displaying limited compatibility with non-polar solvents. As noted, "The solvent environment is crucial in determining the solubility of any given compound," and this compound is no exception.

Interesting facts

Interesting Facts about 2-amino-3-(2-chloroethylsulfanyl)propanoic acid

2-amino-3-(2-chloroethylsulfanyl)propanoic acid, commonly known in scientific literature for its unique structure and properties, is a fascinating compound that has captured the interest of chemists. Here are some intriguing aspects:

  • Amine and Acid Properties: This compound contains both an amine group and a carboxylic acid group, making it a versatile building block. Such dual functionality allows for various chemical reactions and applications in synthesis.
  • Biological Relevance: The presence of the sulfenyl group introduces the possibility of interaction with biological systems, raising interesting questions about its potential biological activity and pharmacological applications.
  • Chirality: The 3-position of this compound introduces chirality, leading to the existence of enantiomers. The study of these can provide insights into molecular interactions and the importance of stereochemistry in biological activity.
  • Synthetic Applications: Researchers value this compound in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique functional groups can serve as intermediates in more complex chemical synthesis.
  • Potential Environmental Impact: Compounds like this, especially those containing chlorine, can be studied to understand their environmental impact. It's essential to assess how such chemicals behave in ecological systems.

As evidenced by its multifaceted characteristics, 2-amino-3-(2-chloroethylsulfanyl)propanoic acid holds promise for future research and practical applications, making it a noteworthy subject in the field of chemistry!

Synonyms
S-(2-Chloroethyl)cysteine
DTXSID10914109
RefChem:180520
DTXCID90874030
2-amino-3-(2-chloroethylsulfanyl)propanoic acid
28361-96-8
S-(2-chloroethyl)-DL-cysteine
S-(2-Chloroethyl)-L-cysteine
S-(2-Chloroethyl)-cysteine
CCRIS 1745
3-((2-Chloroethyl)thio)alanine
BRN 2433353
56674-34-1
ALANINE, 3-((2-CHLOROETHYL)THIO)-
SCHEMBL29048125
97142-17-1
NSC241258
NSC-241258