• 1. An algal process treatment combined with the Fenton reaction for high concentrations of amoxicillin and cefradine
  Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
• 2. An artificial photosynthesis system comprising a covalent triazine framework as an electron relay facilitator for photochemical carbon dioxide reduction?
  Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
• 3. An asymmetric supercapacitor based on controllable WO3 nanorod bundle and alfalfa-derived porous carbon?
  Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
• 4. An approach for correlating the structural and electrical properties of Zr4+-modified SrBi4Ti4O15/SBT ceramic
  Priyambada Nayak,Tanmaya Badapanda,Anil Kumar Singh,Simanchalo Panigrahi RSC Adv., 2017,7, 16319-16331
• 5. An approach to biodegradable star polymeric architectures using disulfide coupling?
  Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds N-arylamides

Comprehensive Guide to Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate (CAS No. 103054-24-6)

Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate (CAS No. 103054-24-6) is a specialized chemical compound widely used in pharmaceutical and agrochemical research. This thiazole derivative is known for its unique structural properties, making it a valuable intermediate in the synthesis of bioactive molecules. With the increasing demand for novel drug candidates and crop protection agents, this compound has garnered significant attention in recent years.

The molecular structure of Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate features a thiazole ring core, which is a common motif in many biologically active compounds. The presence of the chloroacetamido group enhances its reactivity, allowing it to participate in various chemical transformations. Researchers often utilize this compound in the development of antimicrobial agents, anti-inflammatory drugs, and herbicides, aligning with current trends in sustainable agriculture and healthcare.

One of the key advantages of Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate is its versatility in synthetic chemistry. It serves as a building block for the preparation of more complex molecules, particularly in heterocyclic chemistry. The compound's stability under various reaction conditions makes it a preferred choice for laboratories focusing on medicinal chemistry and drug discovery. Recent studies have highlighted its potential in addressing antibiotic resistance, a pressing global health concern.

In the agrochemical sector, Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate is explored for its role in developing eco-friendly pesticides. As the industry shifts toward sustainable practices, this compound's ability to target specific pests without harming beneficial organisms is highly valued. Its application in crop protection formulations is being investigated to meet the growing demand for food security solutions.

The synthesis of Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate typically involves multi-step organic reactions, including amide coupling and esterification. Researchers optimize these processes to achieve high yields and purity, ensuring the compound's suitability for further applications. Advanced techniques such as HPLC and NMR spectroscopy are employed to characterize and validate its structure, meeting stringent quality standards.

From a commercial perspective, the demand for Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate is driven by its relevance in pharmaceutical intermediates and agrochemical research. Suppliers and manufacturers emphasize its high purity and consistent performance, catering to the needs of academic institutions, contract research organizations (CROs), and industrial laboratories. The compound's CAS No. 103054-24-6 is frequently referenced in procurement databases and scientific literature.

Safety and handling guidelines for Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate emphasize standard laboratory precautions. Proper storage conditions, such as maintaining a cool, dry environment, are recommended to preserve its stability. Researchers are advised to consult Material Safety Data Sheets (MSDS) for detailed information on handling and disposal, ensuring compliance with regulatory requirements.

Looking ahead, the potential applications of Methyl 2-[2-(2-Chloroacetamido)-1,3-thiazol-4-yl]acetate continue to expand. Innovations in green chemistry and catalysis may further enhance its utility in sustainable drug development and crop protection. As scientific advancements progress, this compound is poised to play a pivotal role in addressing some of the most critical challenges in healthcare and agriculture.

• 53266-94-7(ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate)
• 64987-03-7(Ethyl 2-(formylamino)-4-thiazoleglyoxylate)
• 75890-68-5(2-(2-Formamidothiazol-4-yl)acetic Acid)
• 64485-82-1(2-(2-Aminothiazole-4-yl)-2-hydroxyiminoacetate)
• 65872-43-7(2-(Formylamino)-1,3-thiazol-4-yl(methoxyimino)acetic acid)
• 64987-05-9(Ethyl 2-(2-formylaminothiazol-4-yl) acetate)
• 64987-06-0(2-(2-Formamidothiazol-4-yl)-2-oxoacetic acid)
• 64987-08-2(ethyl 2-(2-aminothiazol-4-yl)-2-oxo-acetate)
• 73150-67-1(2-(2-aminothiazol-4-yl)-2-oxo-acetic acid)
• 29676-71-9(2-(2-amino-1,3-thiazol-4-yl)acetic acid)