Cas no 216503-31-0 (2-(2-methyloxiran-2-yl)-1,3-thiazole)
2-(2-methyloxiran-2-yl)-1,3-thiazole Chemical and Physical Properties
Names and Identifiers
-
- Thiazole,2-(2-methyl-2-oxiranyl)-
- Thiazole,2-(2-methyloxiranyl)- (9CI)
- 2-(2-methyloxiran-2-yl)-1,3-thiazole
- Thiazole, 2-(2-methyloxiranyl)- (9CI)
- 2-(2-Methyloxiranyl)thiazole
- Thiazole, 2-(2-methyl-2-oxiranyl)-
-
- Inchi: 1S/C6H7NOS/c1-6(4-8-6)5-7-2-3-9-5/h2-3H,4H2,1H3
- InChI Key: DGJPPIRCJMUOOV-UHFFFAOYSA-N
- SMILES: S1C=CN=C1C1(C)CO1
Computed Properties
- Exact Mass: 141.02491
Experimental Properties
- Density: 1.288
- PSA: 25.42
2-(2-methyloxiran-2-yl)-1,3-thiazole Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1844012-0.05g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 0.05g |
$647.0 | 2023-09-19 | ||
| Enamine | EN300-1844012-0.1g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 0.1g |
$678.0 | 2023-09-19 | ||
| Enamine | EN300-1844012-0.25g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 0.25g |
$708.0 | 2023-09-19 | ||
| Enamine | EN300-1844012-0.5g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 0.5g |
$739.0 | 2023-09-19 | ||
| Enamine | EN300-1844012-1.0g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 1g |
$1286.0 | 2023-06-01 | ||
| Enamine | EN300-1844012-2.5g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 2.5g |
$1509.0 | 2023-09-19 | ||
| Enamine | EN300-1844012-5.0g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 5g |
$3728.0 | 2023-06-01 | ||
| Enamine | EN300-1844012-10.0g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 10g |
$5528.0 | 2023-06-01 | ||
| Enamine | EN300-1844012-1g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 1g |
$770.0 | 2023-09-19 | ||
| Enamine | EN300-1844012-5g |
2-(2-methyloxiran-2-yl)-1,3-thiazole |
216503-31-0 | 5g |
$2235.0 | 2023-09-19 |
2-(2-methyloxiran-2-yl)-1,3-thiazole Related Literature
-
Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
-
Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
-
David B. Cordes,Alexandra M. Z. Slawin,Stefania Righetto,Denis Jacquemin,Eli Zysman-Colman,Véronique Guerchais Dalton Trans., 2018,47, 8292-8300
-
Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
-
L. Di Michele,D. Fiocco,F. Varrato,E. Eiser,G. Foffi Soft Matter, 2014,10, 3633-3648
Additional information on 2-(2-methyloxiran-2-yl)-1,3-thiazole
Comprehensive Analysis of 2-(2-methyloxiran-2-yl)-1,3-thiazole (CAS No. 216503-31-0): Properties, Applications, and Industry Trends
The chemical compound 2-(2-methyloxiran-2-yl)-1,3-thiazole (CAS No. 216503-31-0) has garnered significant attention in recent years due to its unique structural features and versatile applications. This heterocyclic molecule combines an epoxide (oxirane) ring with a thiazole moiety, making it a valuable intermediate in pharmaceutical and agrochemical research. The presence of both oxirane and thiazole functional groups allows for diverse reactivity, enabling its use in the synthesis of complex molecules with potential biological activity.
In the context of current industry trends, researchers are increasingly exploring 2-(2-methyloxiran-2-yl)-1,3-thiazole as a building block for drug discovery and crop protection agents. The growing demand for novel heterocyclic compounds in medicinal chemistry has positioned this molecule as a promising candidate for further investigation. Its structural similarity to various bioactive molecules found in nature makes it particularly interesting for pharmaceutical development, especially in areas such as anti-inflammatory and antimicrobial applications.
The synthesis of CAS 216503-31-0 typically involves the reaction of appropriately substituted thiazole precursors with epoxide-forming reagents. Recent advancements in green chemistry have led to improved synthetic routes that minimize waste and reduce environmental impact. These developments align with the current focus on sustainable chemical production, a topic of great interest in both academic and industrial circles. The compound's stability under various conditions makes it suitable for scale-up production, addressing another key concern in modern chemical manufacturing.
From a materials science perspective, 2-(2-methyloxiran-2-yl)-1,3-thiazole has shown potential in the development of advanced functional materials. Its ability to participate in polymerization reactions through the epoxide group opens possibilities for creating novel polymers with specific properties. Researchers are particularly interested in exploring its application in smart coatings and electronic materials, where the combination of thiazole's electronic properties and the reactivity of the epoxide could lead to innovative solutions.
Analytical characterization of CAS 216503-31-0 typically involves techniques such as NMR spectroscopy, mass spectrometry, and X-ray crystallography. These methods confirm the compound's structure and purity, which are critical factors for its successful application in various fields. Recent publications have highlighted novel analytical approaches to study the compound's behavior in different environments, contributing to a better understanding of its structure-activity relationships.
The safety profile of 2-(2-methyloxiran-2-yl)-1,3-thiazole has been the subject of several studies, particularly regarding its handling and storage requirements. While not classified as hazardous under normal conditions, proper laboratory safety protocols should always be followed when working with this compound. The growing emphasis on chemical safety in research and industry makes this aspect particularly relevant for potential users of this chemical.
In the pharmaceutical sector, derivatives of 216503-31-0 are being investigated for their potential biological activity. The thiazole ring is known to interact with various biological targets, and the addition of the epoxide functionality may enhance these interactions or provide new modes of action. This dual functionality makes the compound particularly interesting for medicinal chemistry applications, where researchers are constantly seeking novel scaffolds for drug development.
The agrochemical industry has also shown interest in 2-(2-methyloxiran-2-yl)-1,3-thiazole as a potential precursor for crop protection agents. The need for new pest control solutions that are effective yet environmentally friendly has driven research into novel chemical entities like this one. Its structural features suggest possible activity against various plant pathogens, making it a candidate for further investigation in this field.
From a commercial perspective, the availability of CAS 216503-31-0 from chemical suppliers has increased in recent years, reflecting growing demand. The compound is typically offered in research quantities, with purity levels suitable for various applications. Pricing trends indicate stable availability, though as with many specialty chemicals, market fluctuations can occur based on raw material availability and manufacturing capacity.
Future research directions for 2-(2-methyloxiran-2-yl)-1,3-thiazole may include exploration of its catalytic applications, further investigation of its biological activities, and development of more efficient synthetic routes. The compound's versatility ensures it will remain an important subject of study in multiple chemical disciplines. As the chemical industry continues to evolve, compounds like this that offer multiple functional groups and reactivity patterns will likely play increasingly important roles in both research and industrial applications.
216503-31-0 (2-(2-methyloxiran-2-yl)-1,3-thiazole) Related Products
- 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
- 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
- 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
- 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
- 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
- 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
- 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
- 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
- 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
- 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)