Cas no 881652-46-6 (Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide)
Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide Chemical and Physical Properties
Names and Identifiers
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- Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide
- 3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione
- 3-Methyl-4,5-dihydroisothiazole 1,1-dioxide
- 3-methyl-4,5-dihydro-1,2-thiazole 1,1-dioxide
- SCHEMBL15763048
- AKOS034062758
- 3-methyl-4,5-dihydro-1
- 3-methyl-4,5-dihydro-isothiazole 1,1-dioxide
- Z2831873328
- EN300-395466
- DTXSID301244824
- 881652-46-6
- E?,2-thiazole-1,1-dione
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- Inchi: 1S/C4H7NO2S/c1-4-2-3-8(6,7)5-4/h2-3H2,1H3
- InChI Key: ADXOWPSNHDMYNN-UHFFFAOYSA-N
- SMILES: S1(=O)(=O)CCC(C)=N1
Computed Properties
- Exact Mass: 133.01974964Da
- Monoisotopic Mass: 133.01974964Da
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 8
- Rotatable Bond Count: 0
- Complexity: 209
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -0.6
- Topological Polar Surface Area: 54.9?2
Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| A2B Chem LLC | AX42367-10g |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 10g |
$3979.00 | 2024-04-19 | |
| A2B Chem LLC | AX42367-50mg |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 50mg |
$248.00 | 2024-04-19 | |
| A2B Chem LLC | AX42367-100mg |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 100mg |
$352.00 | 2024-04-19 | |
| A2B Chem LLC | AX42367-250mg |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 250mg |
$489.00 | 2024-04-19 | |
| A2B Chem LLC | AX42367-500mg |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 500mg |
$750.00 | 2024-04-19 | |
| A2B Chem LLC | AX42367-1g |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 1g |
$952.00 | 2024-04-19 | |
| A2B Chem LLC | AX42367-2.5g |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 2.5g |
$1832.00 | 2024-04-19 | |
| A2B Chem LLC | AX42367-5g |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 5g |
$2693.00 | 2024-04-19 | |
| Enamine | EN300-395466-0.05g |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 0.05g |
$202.0 | 2023-07-07 | |
| Enamine | EN300-395466-0.1g |
3-methyl-4,5-dihydro-1lambda6,2-thiazole-1,1-dione |
881652-46-6 | 95% | 0.1g |
$301.0 | 2023-07-07 |
Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide Related Literature
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
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Kaiyuan Huang,Wangkang Qiu,Meilian Ou,Xiaorui Liu,Zenan Liao,Sheng Chu RSC Adv., 2020,10, 18824-18829
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
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Luis Miguel Azofra,Douglas R. MacFarlane,Chenghua Sun Chem. Commun., 2016,52, 3548-3551
Additional information on Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide
Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide (CAS No. 881652-46-6)
Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide is a chemical compound with the CAS registry number 881652-46-6. This compound belongs to the class of heterocyclic compounds known as isothiazoles, which are widely studied for their unique chemical properties and potential applications in various fields. The molecular structure of this compound consists of a five-membered ring containing sulfur and nitrogen atoms, with specific substituents that contribute to its reactivity and functionality.
Recent advancements in the synthesis and characterization of isothiazole derivatives have highlighted their potential in areas such as drug discovery, agrochemicals, and advanced materials. For instance, studies have shown that isothiazole-based compounds can exhibit significant biological activity, making them promising candidates for the development of new pharmaceutical agents. The presence of the dihydro and dioxide groups in this compound further enhances its stability and reactivity, making it a valuable intermediate in organic synthesis.
The synthesis of isothiazole derivatives has been a focal point of research due to their versatility in forming complex molecular architectures. One notable approach involves the reaction of thioamides with carbonyl compounds under specific conditions. This method not only simplifies the synthesis process but also allows for the introduction of various substituents, enabling the creation of tailored structures with desired properties. The dihydro configuration in this compound suggests that it may undergo further oxidation or reduction reactions to yield additional functionalized products.
In terms of applications, isothiazole derivatives have found utility in the development of pesticides and fungicides due to their ability to inhibit key enzymes involved in microbial growth. Recent studies have demonstrated that certain isothiazole-based compounds exhibit potent activity against plant pathogens, offering a sustainable alternative to conventional agrochemicals. Additionally, these compounds are being explored for their potential in catalysis and materials science, where their unique electronic properties can be leveraged to create advanced materials with tailored functionalities.
The environmental impact and safety profile of isothiazole derivatives are critical considerations for their widespread use. Research indicates that these compounds generally exhibit low toxicity to non-target organisms when used at recommended levels. However, ongoing studies are focused on optimizing their formulation and application methods to minimize any potential ecological risks.
In conclusion, Isothiazole, 4,5-dihydro-3-methyl-, 1,1-dioxide (CAS No. 881652-46-6) represents a valuable addition to the arsenal of heterocyclic compounds available for scientific exploration and industrial applications. Its unique chemical structure and versatile reactivity make it a subject of continued interest among researchers across multiple disciplines.
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