Interesting facts
Interesting Facts about 3-Methylsulfanylpropanoic Acid
3-Methylsulfanylpropanoic acid, often simply referred to as a thio acid, presents fascinating characteristics that make it of interest in both organic chemistry and biochemical applications. Here are some noteworthy facts:
- Structure and Properties: This compound features a branched structure due to the methylsulfanyl (–S–CH3) group attached to the propanoic acid backbone. This unique combination allows it to participate in a variety of chemical reactions, particularly those involving sulfur chemistry.
- Biological Relevance: Thio acids, including 3-methylsulfanylpropanoic acid, can often play roles in biological systems. They may be intermediates or products in metabolic pathways, contributing to our understanding of cellular processes.
- Flavor and Aroma: Compounds in the thio acid family, especially those related to sulfur, may impart distinctive flavors and aromas to certain foods. This property makes them interesting candidates for research in food chemistry and flavor chemistry.
- Synthesis: 3-Methylsulfanylpropanoic acid can be synthesized through various methods in organic chemistry, making it a valuable target for synthetic chemists interested in sulfur-containing compounds.
- Pharmaceutical Potential: The unique structure may suggest potential bioactivity. Researchers are exploring how modifications to the thio acid framework could lead to novel pharmaceuticals or therapeutic agents.
As scientists continue to explore the multifaceted roles of such compounds, 3-methylsulfanylpropanoic acid stands out as a prime example of the complexity and beauty inherent in organic chemistry.
Synonyms
3-(Methylthio)propionic acid
646-01-5
3-methylthiopropionate
3-methylthiopropionic acid
3-(Methylthio)propanoic acid
Propanoic acid, 3-(methylthio)-
4-Thiapentanoic acid
3-(Methylsulfanyl)propanoic acid
3-methylsulfanylpropanoic acid
3-methylthiopropanoic acid
3-methylsulfanylpropionic acid
CHEBI:1438
F523ALI47D
Propanoic acid 3-(methylthio)-
3-(Methylmercapto)propionic Acid
Propionic acid, 3-(methylthio)-
3-Methythiopropionic acid
MFCD00059635
3-METHYLTHIOPROPIONA
3-methyl-thiopropionic acid
3-(Methythio)propionic acid
C4H8O2S
3-Methylsulfanyl-Propionic Acid
3-(methyl-sulfanyl)-propanoic acid
3-(methylsulfanyl)propanoate
3-(METHYLMERCAPTO)PROPANOIC ACID
3-(methylthio)propanoate
UNII-F523ALI47D
4-Thiapentanoate
EINECS 211-460-9
3(methylthio)propanoic acid
3-(Methylthio)propionicacid
SCHEMBL342851
CHEMBL116212
DTXSID70862354
3-(Methylsulfanyl)propanoic acid #
LMFA01130006
s6341
AKOS000202219
CS-6296
AS-10364
DA-69853
PD063944
HY-101401
M0811
NS00007379
EN300-16207
C08276
D87669
Q27105456
Z54719251
211-460-9
A8C
Solubility of 3-methylsulfanylpropanoic acid (C4H8O2S)
3-methylsulfanylpropanoic acid is a fascinating compound when it comes to its solubility characteristics. Generally, this compound exhibits a notable level of solubility in various solvents, primarily due to the presence of its functional groups:
In aqueous solutions, 3-methylsulfanylpropanoic acid tends to be more soluble than its non-polar counterparts due to its polar functional groups. However, it's essential to keep in mind:
In summary, the solubility behavior of 3-methylsulfanylpropanoic acid can be summarized as follows:
Understanding these solubility properties can lead to better usage and application of this compound in various fields of chemistry and beyond.