CAS 1822-53-3
:Pyridin-4-Yl-Methanethiol
Description:
Pyridin-4-yl-methanethiol, also known by its CAS number 1822-53-3, is an organic compound characterized by the presence of a pyridine ring substituted with a thiol (-SH) group at the 4-position. This compound typically appears as a colorless to pale yellow liquid with a distinct odor. It is soluble in organic solvents and exhibits moderate solubility in water due to the polar nature of the thiol group. Pyridin-4-yl-methanethiol is known for its reactivity, particularly in nucleophilic substitution reactions, owing to the electron-withdrawing nature of the pyridine ring, which enhances the nucleophilicity of the thiol group. This compound is utilized in various chemical syntheses and can serve as a building block in the development of pharmaceuticals and agrochemicals. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential due to its potential toxicity and reactivity with strong oxidizing agents.
Formula:C6H7NS
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Found 3 products.
4-(Sulfanylmethyl)pyridine
CAS:<p>4-(Sulfanylmethyl)pyridine</p>Purity:≥95%Color and Shape:LiquidMolecular weight:125.19g/mol(Pyridin-4-yl)methanethiol
CAS:<p>Pyridin-4-ylmethanethiol is a molecule that belongs to the class of metalloporphyrins. It has been shown to be a reversible, systematically, and crystallographically covalent tethering ligand for metal ions. Pyridin-4-ylmethanethiol binds reversibly to metal ions such as Cu(II), Fe(III), or Tb(III) and has been shown to inhibit caspase activity in vitro.br>br>Pyridin-4-ylmethanethiol interacts with the supramolecular assembly of the NOD2 protein at the cell membrane, preventing the release of proteases from intracellular vesicles into the extracellular space.</p>Formula:C6H7NSPurity:Min. 95%Molecular weight:125.19 g/mol


