Cas no 1270326-64-1 ((+/-)-1-(3-Amino-pyridin-2-yl)ethylamine)
(+/-)-1-(3-Amino-pyridin-2-yl)ethylamine Chemical and Physical Properties
Names and Identifiers
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- (+/-)-1-(3-Amino-pyridin-2-yl)ethylamine
- 1-(3-Amino-pyridin-2-yl)ethylamine
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- Inchi: 1S/C7H11N3/c1-5(8)7-6(9)3-2-4-10-7/h2-5H,8-9H2,1H3
- InChI Key: JRBZAPCQLIYXQP-UHFFFAOYSA-N
- SMILES: NC(C)C1C(=CC=CN=1)N
Computed Properties
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 10
- Rotatable Bond Count: 1
- Complexity: 105
- Topological Polar Surface Area: 64.9
(+/-)-1-(3-Amino-pyridin-2-yl)ethylamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | A629035-100mg |
(+/-)-1-(3-Amino-pyridin-2-yl)ethylamine |
1270326-64-1 | 100mg |
$ 207.00 | 2023-04-19 | ||
| TRC | A629035-1g |
(+/-)-1-(3-Amino-pyridin-2-yl)ethylamine |
1270326-64-1 | 1g |
$ 1360.00 | 2022-06-07 | ||
| TRC | A629035-1000mg |
(+/-)-1-(3-Amino-pyridin-2-yl)ethylamine |
1270326-64-1 | 1g |
$ 1642.00 | 2023-04-19 |
(+/-)-1-(3-Amino-pyridin-2-yl)ethylamine Related Literature
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
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Jianyao Huang,Dong Gao,Zhihui Chen,Weifeng Zhang Polym. Chem., 2021,12, 2471-2480
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Teresita Carrillo-Hernández,Philippe Schaeffer,Pierre Albrecht Chem. Commun., 2001, 1976-1977
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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
Additional information on (+/-)-1-(3-Amino-pyridin-2-yl)ethylamine
Comprehensive Overview of (+/-)-1-(3-Amino-pyridin-2-yl)ethylamine (CAS No. 1270326-64-1)
(+/-)-1-(3-Amino-pyridin-2-yl)ethylamine (CAS No. 1270326-64-1) is a versatile organic compound with significant applications in pharmaceutical research and chemical synthesis. This chiral amine derivative has garnered attention due to its unique structural properties, which make it a valuable intermediate in the development of drug candidates and biologically active molecules. Its molecular formula, C7H11N3, and amine-functionalized pyridine core contribute to its reactivity and utility in medicinal chemistry.
The compound's racemic mixture form, denoted by the (+/-) prefix, is particularly relevant in asymmetric synthesis and catalysis. Researchers often explore its potential in designing small-molecule inhibitors and ligands for enzyme targeting. Given the rising demand for precision medicine and personalized therapeutics, (+/-)-1-(3-Amino-pyridin-2-yl)ethylamine is frequently discussed in the context of kinase inhibitors and GPCR modulators, aligning with current trends in oncology and neurological drug discovery.
From a synthetic chemistry perspective, this compound serves as a building block for heterocyclic frameworks. Its amino-pyridine moiety is instrumental in constructing nitrogen-rich scaffolds, which are pivotal in agrochemicals and material science. Recent studies highlight its role in covalent organic frameworks (COFs) and metal-organic frameworks (MOFs), addressing the growing interest in sustainable materials and green chemistry.
The CAS No. 1270326-64-1 is often searched alongside terms like "pyridine derivatives in drug design", "chiral amine applications", and "aminoethylpyridine synthesis". These long-tail keywords reflect the compound's niche yet expanding role in R&D. Additionally, its relevance to AI-driven drug discovery and high-throughput screening methodologies has sparked discussions in computational chemistry forums, further boosting its visibility in scientific databases.
Quality control and analytical characterization of (+/-)-1-(3-Amino-pyridin-2-yl)ethylamine are critical for its industrial adoption. Techniques such as HPLC, NMR spectroscopy, and mass spectrometry are employed to ensure purity and consistency, meeting the stringent standards of GMP-compliant production. This aligns with the broader industry shift toward quality-by-design (QbD) principles in fine chemical manufacturing.
In summary, (+/-)-1-(3-Amino-pyridin-2-yl)ethylamine (CAS No. 1270326-64-1) exemplifies the intersection of structural ingenuity and practical utility in modern chemistry. Its applications span life sciences, materials engineering, and catalysis, making it a compound of enduring interest in both academic and industrial settings.
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