Cas no 1356111-01-7 ((5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine)
(5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine Chemical and Physical Properties
Names and Identifiers
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- (5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine
- (5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methamine
- [5-[3-(trifluoromethyl)phenyl]pyridin-3-yl]methanamine
- 1356111-01-7
- 1-{5-[3-(Trifluoromethyl)phenyl]pyridin-3-yl}methanamine
- DTXSID60744377
- DB-223144
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- Inchi: 1S/C13H11F3N2/c14-13(15,16)12-3-1-2-10(5-12)11-4-9(6-17)7-18-8-11/h1-5,7-8H,6,17H2
- InChI Key: ABAGYLUZTBXPCQ-UHFFFAOYSA-N
- SMILES: FC(C1=CC=CC(=C1)C1C=NC=C(CN)C=1)(F)F
Computed Properties
- Exact Mass: 252.08743285g/mol
- Monoisotopic Mass: 252.08743285g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 18
- Rotatable Bond Count: 3
- Complexity: 268
- 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: 2.2
- Topological Polar Surface Area: 38.9?2
(5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A029191499-1g |
(5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine |
1356111-01-7 | 95% | 1g |
$520.00 | 2022-04-03 | |
| Chemenu | CM173017-1g |
(5-(3-(trifluoromethyl)phenyl)pyridin-3-yl)methanamine |
1356111-01-7 | 95% | 1g |
$580 | 2021-08-05 | |
| Chemenu | CM173017-1g |
(5-(3-(trifluoromethyl)phenyl)pyridin-3-yl)methanamine |
1356111-01-7 | 95% | 1g |
$580 | 2022-06-13 |
(5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine Related Literature
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Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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4. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
Additional information on (5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine
Comprehensive Overview of (5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine (CAS No. 1356111-01-7)
The compound (5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine, identified by its CAS No. 1356111-01-7, is a specialized organic molecule that has garnered significant attention in pharmaceutical and agrochemical research. Its unique structural features, including the trifluoromethylphenyl and pyridinylmethanamine moieties, make it a valuable intermediate for developing novel therapeutics and functional materials. Researchers are particularly interested in its potential applications in drug discovery, catalysis, and material science due to its versatile reactivity and stability under various conditions.
In recent years, the demand for fluorinated compounds like (5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine has surged, driven by their enhanced bioavailability and metabolic stability. This aligns with the growing trend in precision medicine and targeted therapy, where such molecules are pivotal for designing small-molecule inhibitors and bioconjugates. The trifluoromethyl group in particular is a hotspot in medicinal chemistry, as it often improves lipophilicity and binding affinity to biological targets.
From a synthetic perspective, CAS No. 1356111-01-7 is often explored for its role in cross-coupling reactions and reductive amination processes. Its pyridine core offers a robust platform for further functionalization, making it a favorite among chemists working on heterocyclic compounds. The compound’s compatibility with green chemistry principles, such as low toxicity and minimal waste generation, further enhances its appeal in sustainable industrial applications.
Another area of interest is the compound’s potential in central nervous system (CNS) drug development. The methanamine moiety is a common pharmacophore in neuroactive agents, and its incorporation into trifluoromethylphenyl-containing scaffolds could lead to breakthroughs in treating neurological disorders. This aligns with current healthcare trends focusing on neurodegenerative diseases like Alzheimer’s and Parkinson’s, where innovative chemical entities are urgently needed.
In the realm of agrochemicals, (5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine is investigated for its herbicidal and insecticidal properties. The trifluoromethyl group is known to enhance the bioactivity of agrochemicals, and this compound’s structural uniqueness positions it as a candidate for next-generation crop protection solutions. With the global push toward sustainable agriculture, such innovations are critical for addressing food security challenges.
Analytical techniques like HPLC, NMR, and mass spectrometry are routinely employed to characterize CAS No. 1356111-01-7, ensuring high purity and consistency for research and industrial use. The compound’s stability under standard storage conditions (e.g., room temperature, inert atmosphere) also makes it a practical choice for laboratories and manufacturing facilities.
As the scientific community continues to explore fluorine chemistry, (5-(3-(Trifluoromethyl)phenyl)pyridin-3-yl)methanamine stands out as a multifaceted building block. Its applications span from life sciences to advanced materials, reflecting the interdisciplinary nature of modern chemical research. Future studies may uncover even broader utilities, solidifying its role in innovation-driven industries.
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