Cas no 947179-20-6 (4-(difluoromethyl)-2-Thiazolamine)
4-(difluoromethyl)-2-Thiazolamine Chemical and Physical Properties
Names and Identifiers
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- 4-(difluoromethyl)-2-Thiazolamine
- 2-Thiazolamine, 4-(difluoromethyl)-
- 4-(Difluoromethyl)-1,3-thiazol-2-amine
- CS-0159065
- 4-Difluoromethyl-thiazol-2-ylamine
- EN300-658533
- 947179-20-6
- SCHEMBL1795530
- BS-42656
- 4-(Difluoromethyl)thiazol-2-amine
-
- Inchi: 1S/C4H4F2N2S/c5-3(6)2-1-9-4(7)8-2/h1,3H,(H2,7,8)
- InChI Key: IEBXYRIXXPDVQO-UHFFFAOYSA-N
- SMILES: S1C(N)=NC(=C1)C(F)F
Computed Properties
- Exact Mass: 150.00632563g/mol
- Monoisotopic Mass: 150.00632563g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 101
- 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: 1.3
- Topological Polar Surface Area: 67.2?2
4-(difluoromethyl)-2-Thiazolamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| eNovation Chemicals LLC | Y1245340-100mg |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95% | 100mg |
$395 | 2024-06-06 | |
| Chemenu | CM542083-1g |
4-(Difluoromethyl)thiazol-2-amine |
947179-20-6 | 95%+ | 1g |
$797 | 2023-01-04 | |
| Enamine | EN300-658533-0.05g |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95.0% | 0.05g |
$864.0 | 2025-03-13 | |
| Enamine | EN300-658533-0.1g |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95.0% | 0.1g |
$904.0 | 2025-03-13 | |
| Enamine | EN300-658533-0.25g |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95.0% | 0.25g |
$946.0 | 2025-03-13 | |
| Enamine | EN300-658533-0.5g |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95.0% | 0.5g |
$987.0 | 2025-03-13 | |
| Enamine | EN300-658533-1.0g |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95.0% | 1.0g |
$1029.0 | 2025-03-13 | |
| Enamine | EN300-658533-2.5g |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95.0% | 2.5g |
$2014.0 | 2025-03-13 | |
| Enamine | EN300-658533-5.0g |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95.0% | 5.0g |
$2981.0 | 2025-03-13 | |
| Enamine | EN300-658533-10.0g |
4-(difluoromethyl)-1,3-thiazol-2-amine |
947179-20-6 | 95.0% | 10.0g |
$4421.0 | 2025-03-13 |
4-(difluoromethyl)-2-Thiazolamine Related Literature
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
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Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
Additional information on 4-(difluoromethyl)-2-Thiazolamine
4-(difluoromethyl)-2-thiazolamine (CAS No. 947179-20-6): A Comprehensive Overview
4-(difluoromethyl)-2-thiazolamine, identified by the CAS registry number 947179-20-6, is a compound of significant interest in various fields of chemistry and material science. This compound, characterized by its unique structure, has garnered attention due to its potential applications in drug development, agrochemicals, and advanced materials. Recent studies have highlighted its role in enhancing the efficiency of chemical reactions and its compatibility with modern synthetic methodologies.
The molecular structure of 4-(difluoromethyl)-2-thiazolamine comprises a thiazole ring with a difluoromethyl substituent at the 4-position and an amine group at the 2-position. This configuration imparts the compound with distinct electronic properties, making it a valuable component in the design of novel chemical systems. The thiazole ring, known for its aromaticity and stability, serves as a versatile scaffold for functionalization, while the difluoromethyl group introduces electron-withdrawing effects that can modulate reactivity in various chemical environments.
Recent research has focused on the synthesis and characterization of 4-(difluoromethyl)-2-thiazolamine. For instance, studies have explored its role as a catalyst in asymmetric synthesis, where it has demonstrated remarkable efficiency in promoting enantioselective reactions. Additionally, investigations into its thermal stability and reactivity under varying conditions have provided insights into its potential use in high-performance materials.
In terms of applications, 4-(difluoromethyl)-2-thiazolamine has shown promise in the development of agrochemicals due to its ability to enhance pest resistance in crops without adverse environmental impacts. Furthermore, its compatibility with biodegradable polymers has opened avenues for its use in sustainable packaging solutions.
The synthesis of 4-(difluoromethyl)-2-thiazolamine typically involves multi-step processes that require precise control over reaction conditions to ensure high yields and purity. Recent advancements in catalytic methods have streamlined these processes, making large-scale production more feasible.
In conclusion, 4-(difluoromethyl)-2-thiazolamine (CAS No. 947179-20-6) stands as a testament to the ongoing innovation in chemical research. Its unique properties and versatile applications underscore its importance as a key compound in contemporary chemistry and material science.
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