53645-99-1 Usage
Uses
Used in Pharmaceutical Industry:
5-CHLORO-4-METHYL-1,2,3-THIADIAZOLE is used as a key intermediate in the synthesis of pharmaceuticals due to its unique chemical structure, which can be further modified to create a range of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 5-CHLORO-4-METHYL-1,2,3-THIADIAZOLE serves as an intermediate for the development of new agrochemicals, potentially enhancing crop protection and yield.
Used in Dye Production:
5-CHLORO-4-METHYL-1,2,3-THIADIAZOLE is used as a building block in the production of dyes, capitalizing on its chemical properties to create a variety of colorants for different applications.
Used as a Corrosion Inhibitor:
5-CHLORO-4-METHYL-1,2,3-THIADIAZOLE is utilized as a corrosion inhibitor, leveraging its chemical composition to protect materials from degradation in various industrial settings.
Used in Organic Synthesis as a Reagent:
5-CHLORO-4-METHYL-1,2,3-THIADIAZOLE is employed as a reagent in organic synthesis, facilitating a range of chemical reactions that contribute to the creation of new organic compounds.
Used in Research:
Its chemical structure and properties make 5-CHLORO-4-METHYL-1,2,3-THIADIAZOLE a valuable tool for research in fields such as medicinal chemistry and materials science, where it aids in the exploration of new chemical pathways and material properties.
Check Digit Verification of cas no
The CAS Registry Mumber 53645-99-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,4 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53645-99:
(7*5)+(6*3)+(5*6)+(4*4)+(3*5)+(2*9)+(1*9)=141
141 % 10 = 1
So 53645-99-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H3ClN2S/c1-2-3(4)7-6-5-2/h1H3
53645-99-1Relevant academic research and scientific papers
Synthesis of lithium 1-alkynesulfenates by the mild oxidation of thiolates with a pinacolone-derived N-sulfonyloxaziridine
Sandrinelli, Franck,Boudou, Cédric,Caupène, Caroline,Averbuch-Pouchot, Marie-Thérèse,Perrio, Stéphane,Metzner, Patrick
, p. 3289 - 3293 (2008/09/18)
Lithium 1-alkynethiolates, generated by a base-induced ring cleavage of 4-substituted 1,2,3-thiadiazoles, were efficiently converted into the corresponding sulfenate salts by mild oxidation using an N-sulfonyloxaziridine derived from pinacolone. In situ S
ON THE REGIOSELECTIVITY IN THE HURD-MORI REACTION
Fujita, Mikako,Kobori, Takeo,Hiyama, Tamejiro,Kondo, Kiyosi
, p. 33 - 36 (2007/10/02)
Various α-substituted (Y) acetone hydrazones were subjected to the Hurd-Mori reaction to give the 4-methyl-5-Y-substituted 1,2,3-thiadiazoles and/or 4-Y-CH2 derivatives.The ratio of the two products changed drastically depending on the kind of the substit
