24367-44-0

Basic information

• Product Name: Pyridine,2-[(1,1-dimethylethyl)dithio]-(9CI)
• Synonyms: Pyridine,2-[(1,1-dimethylethyl)dithio]-(9CI);Pyridine, 2-[(1,1-dimethylethyl)dithio]-
• CAS NO: 24367-44-0
• Molecular Formula: C9H13NS2
• Molecular Weight: 199.33622
• Product Categories: PYRIDINE
• Mol File: 24367-44-0.mol
• Article Data: 24

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Pyridine,2-[(1,1-dimethylethyl)dithio]-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine,2-[(1,1-dimethylethyl)dithio]-(9CI)(24367-44-0)
• EPA Substance Registry System: Pyridine,2-[(1,1-dimethylethyl)dithio]-(9CI)(24367-44-0)

Safety Data

• Hazardous Substances Data: 24367-44-0(Hazardous Substances Data)

Usage

General Description

Pyridine, 2-[(1,1-dimethylethyl)dithio] (9CI) is a chemical compound with the molecular formula C9H15NS. It is a derivative of pyridine with a dithio-substituted tert-butyl group. Pyridine,2-[(1,1-dimethylethyl)dithio]-(9CI) is commonly used in organic synthesis and chemical research as a reagent and catalyst. It is known for its strong pungent odor and is considered to be a highly flammable substance. Pyridine, 2-[(1,1-dimethylethyl)dithio] (9CI) is also known to have potential toxic effects on human health and should be handled and used with caution in controlled laboratory settings.

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Relevant articles and documents

Catalyst-free Synthesis of 2-(tert-Butyldisulfanyl) Heterocycles from tert-Butanesulfinamide and Mercapto-substituted Imidazoles, Tetrazole, Pyrimidine and Pyridine

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Visible-light photocatalytic selective aerobic oxidation of thiols to disulfides on anatase TiO2

This work presents the visible-light photocatalytic selective oxidation of thiols to disulfides with molecular oxygen (O2) on anatase TiO2. The high specific surface area of anatase TiO2 proved to be especially critical in

Phototropin-Inspired Chemoselective Synthesis of Unsymmetrical Disulfides: Aerobic Oxidative Heterocoupling of Thiols Using Flavin Photocatalysis

Inspired by the photochemical mechanism of a plant blue-light receptor, a unique flavin-based photocatalytic system was developed for the chemoselective heterocoupling of two different thiols, which enabled the facile synthesis of unsymmetrical disulfides. Owing to the redox- and photo-organocatalysis of flavin, the coupling reaction took place under mild metal-free conditions and visible light irradiation with the use of air, which is recognized as the ideal green oxidant.