Interesting facts
Interesting Facts about Methyl 2-amino-3-sulfanyl-propanoate; Hydrochloride
Methyl 2-amino-3-sulfanyl-propanoate; hydrochloride is a fascinating compound that stands out in the realm of organic chemistry. Here are some intriguing aspects:
- Biological Significance: This compound is often studied for its role in medicinal chemistry, specifically as it can act as a precursor for various biologically active molecules. The presence of both an amino group and a sulfanyl group makes it a potential candidate for drug synthesis.
- Research Applications: Due to its unique structure, researchers investigate its potential applications in the field of antioxidants and anti-inflammatory agents, making it of significant interest for pharmaceutical research.
- Versatile Reactivity: The amino and sulfanyl functionalities allow this compound to participate in a range of chemical reactions, including nucleophilic substitutions and coupling reactions. This versatility is crucial for synthesizing larger, more complex molecules.
- Hydrochloride Form: The hydrochloride salt form enhances the solubility of the compound, making it easier to handle in laboratory settings and in biological studies. This is particularly beneficial when preparing solutions for experimentation.
- Structural Diversity: The presence of multiple functional groups in its structure allows for the exploration of various chemical properties. This complexity can lead to unexpected interactions and potential new research avenues.
Overall, Methyl 2-amino-3-sulfanyl-propanoate; hydrochloride exemplifies how simple modifications in chemical structure can yield profound implications in biological systems and organic synthesis. In the words of renowned chemists, "The beauty of chemistry lies in the vast possibilities of combinations," which certainly applies to this compound!
Synonyms
5714-80-7
Cysteine, methyl ester, hydrochloride
Cysteine, methyl ester, hydrochloride (1:1)
EINECS 227-208-6
Cysteine, methyl ester, hydrochloride (VAN)
methyl 2-amino-3-mercaptopropanoate hydrochloride
Methyl 2-amino-3-mercaptopropionate hydrochloride
Methyl 2-amino-3-mercaptopropanoate, HCl
Methyl DL-cysteinate hydrochloride
methyl 2-amino-3-sulfanylpropanoate hydrochloride
Methyl2-amino-3-mercaptopropanoate,HCl
MFCD00173915
methyl cysteinate hydrochloride
MFCD00038985
MFCD00672724
DL-Cysteine methyl ester hydrochloride
H-D-Cys-OMe HCl
Cysteine, hydrochloride
Methyl cysteine, hydrochloride
SPECTRUM1500636
SCHEMBL1445530
CHEMBL1490495
DTXSID90972606
WHOHXJZQBJXAKL-UHFFFAOYSA-N
HMS1921M13
Pharmakon1600-01500636
BCP30482
CCG-39983
NSC161611
NSC757395
AKOS008966901
NSC-757395
NCGC00094821-01
NCGC00094821-02
BS-17674
DA-55384
SY021999
SY076955
SY131689
Methyl .beta.-mercaptoalanine hydrochloride
D-Cysteine,methyl ester,hydrochloride(1:1)
DB-044575
DB-360663
CS-0150913
Methyl cysteinate--hydrogen chloride (1/1)
EN300-05974
H10905
Methyl2-amino-3-mercaptopropionatehydrochloride
methyl 2-amino-3-sulfanylpropanoate;hydrochloride
Methyl .alpha.-amino-.beta.-mercaptopropionate hydrochloride
Mecysteine hydrochloride pound>>Methyl cysteine hydrochloride ; Mecysteine HCl; NSC 161611; NSC161611; NSC-161611
Solubility of Methyl 2-amino-3-sulfanyl-propanoate Hydrochloride
Methyl 2-amino-3-sulfanyl-propanoate; hydrochloride is an intriguing compound when considering its solubility potential. Generally, the solubility of a compound is influenced by several factors, including its chemical structure, polarity, and the nature of its functional groups.
For this specific compound, we can make the following observations:
As a concluding note, one might expect that methyl 2-amino-3-sulfanyl-propanoate; hydrochloride would display a relatively high solubility in water, largely due to its ionic nature and polar functionalities. This is particularly useful in various applications, where solubility plays a crucial role in the reactivity and bioavailability of compounds.