Interesting facts
Interesting Facts about (2S)-2-amino-4,4-dichloro-butanoic acid
(2S)-2-amino-4,4-dichloro-butanoic acid, commonly referred to in the scientific community as a unique amino acid derivative, has garnered attention due to its intriguing properties and applications. Here are some key points that highlight its significance:
- Chiral Nature: This compound possesses a stereogenic center, making it chiral. The 2S designation indicates the specific spatial arrangement of its atoms, which is a crucial aspect in the study of molecular interactions and pharmacology.
- Role in Drug Design: Amino acid derivatives like this one often serve as building blocks in pharmaceutical chemistry, leading to the design of novel drugs with enhanced efficacy and reduced side effects.
- Potential Antimetabolite: The presence of dichloro groups suggests potential antimetabolite activity, which can inhibit vital metabolic processes in certain microorganisms. This property might be exploited in developing antimicrobial agents.
- Research Applications: Scientists are exploring the behavior of this compound in various biochemical pathways, contributing to a better understanding of protein synthesis and enzymatic reactions.
- Environmental Impact: Due to its structure, studies are underway investigating its environmental stability and potential effects in ecological systems, highlighting the importance of understanding chemical interactions in our surroundings.
In summary, (2S)-2-amino-4,4-dichloro-butanoic acid exemplifies the complex interplay between structure and function in chemistry, embodying both the challenges and opportunities faced by researchers today. As the landscape of drug development and environmental science evolves, compounds like this will undoubtedly play a pivotal role.
Synonyms
Armentomycin
10139-00-1
(S)-2-Amino-4,4-dichlorobutanoic acid
(2S)-2-amino-4,4-dichlorobutanoic acid
Antibiotic U 10923
L-2-Amino-4,4-dichlorobutyric acid
alpha,alpha-Dichloro-L-butyrine
Butyric acid, 2-amino-4,4-dichloro-, L-
U-10923
BUTANOIC ACID, 2-AMINO-4,4-DICHLORO-, (S)-
alpha alpha-dichloro-L-butyrine
(2S)-2-Amino-4,4-dichlorobutanoate
Butyric acid, 2-amino-4,4-dichloro-, L-(8CI)
2-Amino-4,4-dichlorobutanoic acid
SCHEMBL2923837
DTXSID60906115
CHEBI:221029
DGJTWBMINQYSMS-REOHCLBHSA-N
AKOS006277422
(2S)-2-amino-4,4-dichloro-butanoic acid
HY-113569
Solubility of (2S)-2-amino-4,4-dichloro-butanoic acid
(2S)-2-amino-4,4-dichloro-butanoic acid, also known as a chlorinated amino acid, exhibits unique solubility characteristics that are of particular interest. The presence of both amino and carboxylic acid functional groups in its structure significantly influences its solubility behavior in different solvents.
Factors Affecting Solubility
The solubility of this compound can be affected by several key factors:
Solubility in Different Solvents
In terms of specific solubility:
As noted, the solubility behavior of (2S)-2-amino-4,4-dichloro-butanoic acid is a notable characteristic that reflects the molecular interactions between the compound and solvent systems, making it crucial for various applications where solubility plays a key role.