sodium 5-(1,2-dithiolan-3-yl)pentanoate
$200.00
CAS No.: 2319-84-8
Catalog No.: 197705
Purity: 95%
MF: C8H13NaO2S2
MW: 228.314
Storage: 2-8 degree Celsius
SMILES: S1SC(CC1)CCCCC(=O)[O-].[Na+]
Catalog No.: 197705
Purity: 95%
MF: C8H13NaO2S2
MW: 228.314
Storage: 2-8 degree Celsius
SMILES: S1SC(CC1)CCCCC(=O)[O-].[Na+]
sodium 5-(1,2-dithiolan-3-yl)pentanoate; CAS No.: 2319-84-8;sodium 5-(1,2-dithiolan-3-yl)pentanoate. PROPERTIES: Sodium 5-(1,2-dithiolan-3-yl)pentanoate is a sodium salt of a dithiolane-containing carboxylic acid with a molecular weight of 222.32 g/mol. This white crystalline solid has a melting point between 145-148 C. The molecule features a 1,2-dithiolane ring substituted with a pentanoate chain at position 3, forming a sodium salt. It demonstrates limited solubility in common organic solvents such as ethanol and acetone but is sparingly soluble in water. Proper storage involves keeping in tightly sealed containers at room temperature, protected from light and moisture. Safety considerations include the dithiolane ring's potential to release sulfur oxides when heated and the general toxicity of the sodium salt. Standard laboratory safety protocols should be observed. APPLICATIONS: This compound primarily functions as a building block in the synthesis of agrochemicals and pharmaceuticals, where the dithiolane group provides structural diversity for receptor interactions. In medicinal chemistry, it has been employed in developing antimicrobial agents targeting bacterial infections and has shown utility in creating antioxidants for pharmaceutical applications. The dithiolane-pentanoate structure has also been explored in materials science for developing chiral ligands in asymmetric catalysis, leveraging the sulfur atoms' stereoelectronic effects. These applications are documented in publications from the Journal of Medicinal Chemistry and the Journal of Catalysis.
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