CAS 2044-73-7

2-Pyridinemethanethiol

Description:

2-Pyridinemethanethiol, also known as 2-(methylthio)pyridine, is an organic compound characterized by the presence of a pyridine ring substituted with a thiol group. Its molecular structure features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and a methanethiol group (-CH2SH) attached to the second carbon of the ring. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents and exhibits moderate solubility in water. 2-Pyridinemethanethiol is known for its potential applications in organic synthesis, particularly as a building block in the preparation of various pharmaceuticals and agrochemicals. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety considerations include its potential irritant properties, and appropriate handling measures should be taken to minimize exposure. Overall, 2-Pyridinemethanethiol is a versatile compound with significant relevance in chemical research and industry.

Formula: C₆H₇NS

InChI: InChI=1S/C6H7NS/c8-5-6-3-1-2-4-7-6/h1-4,8H,5H2

InChI key: InChIKey=SJIIDWBFRZACDQ-UHFFFAOYSA-N

SMILES: C(S)C1=CC=CC=N1

Synonyms:

• 2-(Mercaptomethyl)pyridine
• 2-Picolylthiol
• 2-Pyridinemethanethiol
• 2-Pyridylmethanethiol
• 2-Pyridylmethyl mercaptan
• NSC 82320
• Pyridin-2-Ylmethanethiol
• Pyridine-2-thiocarbinol

2-Pyridinemethanethiol

CAS: 2044-73-7

Formula: C₆H₇NS

Purity: 95%

Color and Shape: Liquid

Molecular weight: 125.1915

Ref: IN-DA0029HE

2-(Sulphanylmethyl)pyridine

CAS: 2044-73-7

2-(Sulphanylmethyl)pyridine

Purity: ≥95%

Molecular weight: 125.19g/mol

Ref: 54-OR305407

Pyridin-2-ylmethanethiol

CAS: 2044-73-7

Formula: C₆H₇NS

Purity: 95%

Color and Shape: Liquid, Oil

Molecular weight: 125.19

Ref: 10-F461521

2-(Sulphanylmethyl)pyridine

CAS: 2044-73-7

2-(Sulphanylmethyl)pyridine is a stabilizer that can be used in fatty acids. It is a reversible covalent bond that can stabilize the sample by reacting with the phosphorothioates of nucleic acids and other nucleophiles, such as sulphydryl groups. 2-(Sulphanylmethyl)pyridine reacts with glycerides to form reaction products, which may be used as additives for oils or fats. This product has been shown to have potential for use in X-ray crystallography studies of phosphorothioates. 2-(Sulphanylmethyl)pyridine stabilizes metal ions and can be used orally as acetyl derivatives.

Formula: C₆H₇NS

Purity: Min. 95%

Molecular weight: 125.19 g/mol

Ref: 3D-CAA04473