Cas no 454-99-9 (2,4-Bis(trifluoromethyl)pyridine)
2,4-Bis(trifluoromethyl)pyridine Chemical and Physical Properties
Names and Identifiers
-
- 2,4-Bis(trifluoromethyl)pyridine
- Pyridine, 2,4-bis(trifluoromethyl)-
- NZFDZFJVWFDFQV-UHFFFAOYSA-N
- 2,4-Bis(trifluoromethyl)pyridine #
- BBL103917
- STL557727
-
- MDL: MFCD03093758
- Inchi: 1S/C7H3F6N/c8-6(9,10)4-1-2-14-5(3-4)7(11,12)13/h1-3H
- InChI Key: NZFDZFJVWFDFQV-UHFFFAOYSA-N
- SMILES: FC(C1C=CN=C(C(F)(F)F)C=1)(F)F
Computed Properties
- Exact Mass: 215.017
- Monoisotopic Mass: 215.017
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 7
- Heavy Atom Count: 14
- Rotatable Bond Count: 0
- Complexity: 195
- 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: 2.7
- Topological Polar Surface Area: 12.9
2,4-Bis(trifluoromethyl)pyridine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A029002529-250mg |
2,4-Bis(trifluoromethyl)pyridine |
454-99-9 | 95% | 250mg |
$940.80 | 2023-09-01 | |
| Alichem | A029002529-500mg |
2,4-Bis(trifluoromethyl)pyridine |
454-99-9 | 95% | 500mg |
$1617.60 | 2023-09-01 | |
| Alichem | A029002529-1g |
2,4-Bis(trifluoromethyl)pyridine |
454-99-9 | 95% | 1g |
$2837.10 | 2023-09-01 | |
| TRC | B191120-50mg |
2,4-Bis(trifluoromethyl)pyridine |
454-99-9 | 50mg |
$ 185.00 | 2022-06-07 | ||
| TRC | B191120-100mg |
2,4-Bis(trifluoromethyl)pyridine |
454-99-9 | 100mg |
$ 295.00 | 2022-06-07 | ||
| TRC | B191120-250mg |
2,4-Bis(trifluoromethyl)pyridine |
454-99-9 | 250mg |
$ 590.00 | 2022-06-07 | ||
| Matrix Scientific | 202286-0.250g |
2,4-Bis(trifluoromethyl)pyridine, 95% |
454-99-9 | 95% | 0.250g |
$205.00 | 2023-09-07 | |
| Matrix Scientific | 202286-0.500g |
2,4-Bis(trifluoromethyl)pyridine, 95% |
454-99-9 | 95% | 0.500g |
$341.00 | 2023-09-07 | |
| Matrix Scientific | 202286-1g |
2,4-Bis(trifluoromethyl)pyridine, 95% |
454-99-9 | 95% | 1g |
$568.00 | 2023-09-07 | |
| Apollo Scientific | PC520525-1g |
2,4-Bis(trifluoromethyl)pyridine |
454-99-9 | 95% | 1g |
£400.00 | 2023-09-02 |
2,4-Bis(trifluoromethyl)pyridine Related Literature
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
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Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
Additional information on 2,4-Bis(trifluoromethyl)pyridine
2,4-Bis(trifluoromethyl)pyridine: A Comprehensive Overview
2,4-Bis(trifluoromethyl)pyridine, also known by its CAS number 454-99-9, is a highly specialized organic compound that has garnered significant attention in various fields of chemistry and materials science. This compound belongs to the family of pyridines, which are six-membered aromatic heterocycles containing one nitrogen atom. The presence of two trifluoromethyl groups at the 2 and 4 positions of the pyridine ring imparts unique electronic and structural properties to this molecule, making it a valuable component in numerous applications.
The synthesis of 2,4-Bis(trifluoromethyl)pyridine involves a multi-step process that typically begins with the preparation of a suitable precursor. One common approach is the use of amines or amides as starting materials, followed by cyclization reactions under specific conditions to form the pyridine ring. The introduction of trifluoromethyl groups is achieved through electrophilic substitution or other advanced techniques, ensuring precise regioselectivity. Recent advancements in catalytic methods have significantly improved the efficiency and yield of this synthesis, making it more accessible for large-scale production.
The electronic properties of 2,4-Bis(trifluoromethyl)pyridine are heavily influenced by the electron-withdrawing trifluoromethyl groups. These groups not only enhance the stability of the molecule but also modulate its reactivity in various chemical transformations. For instance, the compound exhibits excellent thermal stability, which is crucial for applications in high-temperature environments. Additionally, its ability to act as an electron-deficient aromatic system makes it an attractive candidate for use in electrophilic aromatic substitution reactions.
In terms of applications, 2,4-Bis(trifluoromethyl)pyridine has found extensive use in the field of materials science. It serves as a building block for constructing advanced materials such as organic semiconductors and functional polymers. Recent studies have demonstrated its potential in enhancing the electrical conductivity and mechanical stability of polymer blends, making it a valuable additive in high-performance materials.
The compound also plays a pivotal role in pharmaceutical research. Its unique electronic properties make it an ideal candidate for designing bioactive molecules with specific pharmacological profiles. Researchers have explored its use as a scaffold for developing drugs targeting various diseases, including cancer and neurodegenerative disorders. The trifluoromethyl groups contribute to improved bioavailability and selectivity, which are critical factors in drug design.
In addition to its role in materials science and pharmacology, 2,4-Bis(trifluoromethyl)pyridine has been utilized in catalysis and sensor technology. Its ability to act as a ligand in transition metal complexes has led to the development of highly efficient catalysts for organic transformations. Furthermore, its responsiveness to environmental stimuli makes it suitable for designing sensors capable of detecting changes in pH or temperature.
The latest research on 2,4-Bis(trifluoromethyl)pyridine has focused on expanding its application scope while improving its synthesis methods. Scientists are exploring green chemistry approaches to reduce waste and improve sustainability in its production process. Additionally, there is growing interest in understanding its interaction with biological systems at a molecular level to unlock new therapeutic possibilities.
In conclusion, 2,4-Bis(trifluoromethyl)pyridine, with its CAS number 454-99-9, stands out as a versatile compound with immense potential across multiple disciplines. Its unique chemical properties and diverse applications continue to drive innovative research and development efforts worldwide.
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