21036-67-9 Usage
Uses
Used in Pharmaceutical Industry:
2-METHYL-4-(2-THIENYL)-1,3-THIAZOLE is utilized as a building block in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, particularly those with antimicrobial and anticancer properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-METHYL-4-(2-THIENYL)-1,3-THIAZOLE serves as an intermediate in the production of agrochemicals. Its incorporation into these compounds can enhance their effectiveness in pest control and crop protection.
Used in Material Science:
2-METHYL-4-(2-THIENYL)-1,3-THIAZOLE is also employed in material science for the synthesis of new materials with specific properties. Its heterocyclic nature can contribute to the development of materials with improved characteristics for various applications.
Used in Dye and Pigment Production:
As an intermediate in the production of dyes and pigments, 2-METHYL-4-(2-THIENYL)-1,3-THIAZOLE plays a crucial role in creating organic compounds with vibrant colors and stable properties for use in various industries, including textiles, plastics, and printing inks.
Used in Organic Compounds Synthesis:
2-METHYL-4-(2-THIENYL)-1,3-THIAZOLE is used as an intermediate in the synthesis of other organic compounds. Its presence in these compounds can impart specific chemical and physical properties, making it valuable in a wide range of chemical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 21036-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,3 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21036-67:
(7*2)+(6*1)+(5*0)+(4*3)+(3*6)+(2*6)+(1*7)=69
69 % 10 = 9
So 21036-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NS2/c1-6-9-7(5-11-6)8-3-2-4-10-8/h2-5H,1H3
21036-67-9Relevant academic research and scientific papers
Access to Thiazole via Copper-Catalyzed [3+1+1]-Type Condensation Reaction under Redox-Neutral Conditions
Tang, Xiaodong,Yang, Jidan,Zhu, Zhongzhi,Zheng, Meifang,Wu, Wanqing,Jiang, Huanfeng
, p. 11461 - 11466 (2016/11/28)
A new strategy for thiazoles via copper-catalyzed [3+1+1]-type condensation reaction from oximes, anhydrides and potassiumthiocyanate (KSCN) is developed herein. The transformation has good functional group tolerance and various thiazoles were formed smoothly in good to excellent yields under mild reaction conditions. This process involves copper-catalyzed N-O/C-S bond cleavages, activation of vinyl sp2 C-H bond, and C-S/C-N bond formations which are under redox-neutral conditions as well as operational simplicity.
Xi:Irritant;
