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L-Alliin

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Identification
Molecular formula
C6H10Cl2NO2S
CAS number
556-27-4
IUPAC name
(2R)-2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid
State
State

At room temperature, L-Alliin is typically a solid.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.20
Boiling point (Celsius)
276.70
Boiling point (Kelvin)
549.90
General information
Molecular weight
177.63g/mol
Molar mass
177.6340g/mol
Density
1.2810g/cm3
Appearence

L-Alliin is a crystalline solid that is colorless to pale yellow. It may appear as a powder or crystalline aggregated form.

Comment on solubility

Solubility of (2R)-2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid

The solubility of (2R)-2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid can be fascinating to explore due to its unique structure and functional groups. Understanding its solubility characteristics involves considering several factors:

  • Polarity: This compound contains both amino (–NH2) and carboxyl (–COOH) groups, which generally increase its polarity and ability to interact with polar solvents, such as water.
  • Presence of Chlorine: The two chlorine atoms in the compound may introduce additional polarity but also steric hindrance, influencing solubility in organic solvents.
  • Acid-Base Properties: The carboxylic acid functionality allows for proton donation, which can enhance solubility in basic media.
  • Hydrophilicity vs. Hydrophobicity: The presence of the dichlorovinylsulfanyl group suggests some hydrophobic character, potentially limiting solubility in purely aqueous environments.
  • Temperature Dependence: Like many organic compounds, solubility may increase with temperature due to enhanced molecular motion.

In summary, one could expect that the solubility of (2R)-2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid would be greater in polar solvents, particularly under conditions that promote ionization of its acidic group. However, challenges may arise in purely aqueous environments due to the hydrophobic influences from the chlorinated vinyl moiety. As always, empirical testing reveals the most accurate solubility profile.

Interesting facts

Interesting Facts about (2R)-2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid

(2R)-2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid, commonly known for its unique structure and properties, is an intriguing compound that contributes to various fields of chemistry and biology. Here are some engaging insights into this fascinating molecule:

  • Structural Significance: The presence of a dichlorovinyl group in its structure highlights its potential in medicinal chemistry, particularly in designing drugs that target specific biological pathways.
  • Biological Relevance: This compound may act as a biochemical agent, participating in crucial metabolic processes within cells. Its amino acid framework suggests potential roles in protein synthesis or modulation of enzymatic activities.
  • Research Interest: Scientists are particularly interested in the reactivity of compounds with similar structures, often exploring their capacity as inhibitors or activators in various biochemical reactions.
  • Environmental Impact: Compounds containing dichlorovinyl groups can be significant in environmental studies, as they can influence ecological systems and deserve careful evaluation regarding their persistence and degradation.
  • Potential Applications: With its complex structure, (2R)-2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid could pave the way for innovative solutions in pharmaceuticals, agrochemicals, and synthetic biology.

As researchers continue to investigate this compound, its full potential remains to be unlocked. As with many synthetic chemicals, understanding its behavior and interactions will be crucial for future developments.

Synonyms
S-(1,2-Dichlorovinyl)-L-cysteine
S-(E-1,2-DICHLOROVINYL)-L-CYSTEINE
(2R)-2-Amino-3-(1,2-dichloroethenylsulfanyl)propanoic acid
DTXSID001301340
13419-46-0
DB-262024
Q27120670