1822-53-3 Usage
Uses
Used in Pharmaceutical Industry:
PYRIDIN-4-YL-METHANETHIOL is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the design of new drugs, enhancing their therapeutic properties and effectiveness in treating different medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, PYRIDIN-4-YL-METHANETHIOL is utilized as a precursor in the synthesis of agrochemicals. Its presence in these compounds contributes to their pesticidal, herbicidal, or insecticidal properties, thereby supporting agricultural productivity and crop protection.
Used as a Reagent in Chemical Reactions:
PYRIDIN-4-YL-METHANETHIOL serves as a reagent in various chemical reactions, facilitating the synthesis of complex organic compounds. Its reactivity and functional groups make it a valuable tool in organic chemistry, enabling the formation of new chemical bonds and the modification of existing ones.
Used as a Building Block for Organic Compounds:
PYRIDIN-4-YL-METHANETHIOL is employed as a building block in the construction of diverse organic compounds. Its structural features allow it to be a component of larger molecules, contributing to the development of new materials and compounds with specific properties and applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1822-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1822-53:
(6*1)+(5*8)+(4*2)+(3*2)+(2*5)+(1*3)=73
73 % 10 = 3
So 1822-53-3 is a valid CAS Registry Number.
1822-53-3Relevant academic research and scientific papers
On the reduction mechanism of thionicotinamide and thioisonicotinamide on mercury electrodes in strongly acidic media
Montoya, Mercedes Ruiz,Galvin, Rafael Marin,Mellado, Jose Miguel Rodriguez
, p. 19 - 22 (2007/10/03)
The electroreduction of thionicotinamide (TNA) and thioisonicotinamide (TINA) has been studied in aqueous acidic media (pH + ion was transferred prior to the r.d.s., and the intermediate was formed after the uptake of a second proton.For TINA, the uptake of two electrons and two H+ ions to form the intermediate appeared as reversible.The intermediate can experience two alternative (and parallel) processes; a protonation or an elimination of either SH2 or NH3.The limiting currents of the waves are partially controlled by these chemical reactions, and the different dependence of their rates with the acidity of the medium is responsible for the dependence of the limiting current on pH. - Key words: Reduction mechanisms; Thionicotinamide; Thioisonicotinamide; Polarography; Voltammetry
