14066-76-3

Basic information

• Product Name: 2(3H)-Thiazolethione, 5-[2-(acetyloxy)ethyl]-4-Methyl-
• Synonyms: 2(3H)-Thiazolethione, 5-[2-(acetyloxy)ethyl]-4-Methyl-;4-methyl-5-(β-acetoxyethyl)-2-thiazolinethione
• CAS NO: 14066-76-3
• Molecular Formula: C₈H₁₁NO₂S₂
• Molecular Weight: 217.30844
• Mol File: 14066-76-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2(3H)-Thiazolethione, 5-[2-(acetyloxy)ethyl]-4-Methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Thiazolethione, 5-[2-(acetyloxy)ethyl]-4-Methyl-(14066-76-3)
• EPA Substance Registry System: 2(3H)-Thiazolethione, 5-[2-(acetyloxy)ethyl]-4-Methyl-(14066-76-3)

Safety Data

• Hazardous Substances Data: 14066-76-3(Hazardous Substances Data)

Usage

Structure

Contains a thiazole ring with a sulfur and nitrogen atom, and a methyl and acetyloxyethyl group attached to the ring

Usage

Synthesis of pharmaceuticals and agricultural products, organic and medicinal chemistry research, potential applications as a fungicide and in the development of new drugs

Safety

Should be handled with care and proper safety procedures must be followed, as it can be hazardous if not handled properly.

Upstream product

• 513-74-6 ammonium dithiocarbamate 
• 13051-49-5 5-Acetoxy-3-chloropentan-2-one 
• 2986-00-7 3-acetyl-3-chlorodihydrofuran-2(3H)-one 
• 1124-01-2 5-(2-hydroxy-ethyl)-4-methyl-3H-thiazole-2-thione 
• 108-24-7 acetic anhydride 
• 408340-34-1 4-hydroxy-5-(2-hydroxy-ethyl)-4-methyl-thiazolidine-2-thione 
• 58371-98-5 3, 5-dichloro-2-pentanone 
• 13045-13-1 3-chloro-3-acetylpropanol 

Downstream Products

• 656-53-1 acetic acid 2-(4-methyl-thiazol-5-yl)-ethyl ester 
• 137-00-8 5-hydroxyethyl-4-methylthiazole 

Relevant articles and documents

Synthetic method of thiazoles (by machine translation)

4 - Acetoxy 3 - acetyl -3 - chloropropyl acetate is hydrolyzed under acidic conditions to prepare 4 -mercapto -2 - methyl -2 - (β - acetoxyethyl)-thiazole; the step of preparing -2 - methyl -2 - (β - acetoxyethyl)-thiazole with 3 - methyl -3 - (β - acetoxyethyl)-thiazole under acidic condition is carried out under an acidic condition by adding an oxidizing agent under an acidic condition in 3 -chloro -3 -methyl 2 - (β - acetoxyethyl)-thiazole in an acidic condition under an acidic condition by adding 4 - an oxidizing agent under an acidic condition; and a -5 - method -5 - for synthesizing thiazoles -4 - and -5 -mercapto 2 -methyl-ethyl)-thiazole in an acidic condition by adding an -5 - oxidizing agent under an -5 - 4 - acidic condition; and the method comprises the following steps: preparing -4 -4 - ethyl acetoxyethyl)-thiazole. The synthesis method is mild in overall reaction condition, simple in post-treatment and suitable for pilot scale test and industrial production. (by machine translation)