Cas no 138113-09-4 (2-(7-methoxynaphthalen-1-yl)ethan-1-amine)
2-(7-methoxynaphthalen-1-yl)ethan-1-amine Chemical and Physical Properties
Names and Identifiers
-
- 2-(7-Methoxynaphthalen-1-yl)ethanamine
- 2-(7-Methoxy-1-naphthyl)ethanamine
- 2-(7-Methoxynaphth-1-yl)ethylamine
- 7-methoxy-1-Naphthaleneethanamine
- 1-naphthaleneethanamine, 7-methoxy-
- LogP
- 2-(7-methoxynaphthalen-1-yl)ethan-1-amine
- DB-063232
- YXDUMIVUPSVYLB-UHFFFAOYSA-N
- SCHEMBL124465
- CS-0445795
- (7-methoxy-1-naphthyl)ethyl amine
- 2-(7-Methoxy-naphthalen-1-yl)-ethylamine
- AKOS015998974
- E84643
- 2-(7-METHOXY-1-NAPHTHYL)ETHYLAMINE
- EN300-9404889
- DTXSID00453436
- 138113-09-4
- TS-01498
- MFCD09744147
- BCP15348
-
- MDL: MFCD09744147
- Inchi: 1S/C13H15NO/c1-15-12-6-5-10-3-2-4-11(7-8-14)13(10)9-12/h2-6,9H,7-8,14H2,1H3
- InChI Key: YXDUMIVUPSVYLB-UHFFFAOYSA-N
- SMILES: O(C)C1C=CC2=CC=CC(CCN)=C2C=1
Computed Properties
- Exact Mass: 201.11545
- Monoisotopic Mass: 201.115364102g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 15
- Rotatable Bond Count: 3
- 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: 2.5
- Topological Polar Surface Area: 35.2?2
Experimental Properties
- Density: 1.093
- PSA: 35.25
2-(7-methoxynaphthalen-1-yl)ethan-1-amine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A219005575-1g |
2-(7-Methoxynaphthalen-1-yl)ethanamine |
138113-09-4 | 95% | 1g |
998.00 USD | 2021-06-15 | |
| Chemenu | CM140924-1g |
2-(7-Methoxy-1-naphthyl)ethanamine |
138113-09-4 | 95% | 1g |
$482 | 2021-08-05 | |
| Apollo Scientific | OR315746-1g |
2-(7-Methoxynaphthalen-1-yl)ethanamine |
138113-09-4 | 95 | 1g |
£50.00 | 2025-02-19 | |
| Chemenu | CM140924-1g |
2-(7-Methoxy-1-naphthyl)ethanamine |
138113-09-4 | 95% | 1g |
$*** | 2023-03-30 | |
| abcr | AB540293-1 g |
2-(7-Methoxy-1-naphthyl)ethanamine; . |
138113-09-4 | 1g |
€368.80 | 2023-04-14 | ||
| 1PlusChem | 1P0018HF-100mg |
1-Naphthaleneethanamine, 7-methoxy- |
138113-09-4 | 95% | 100mg |
$72.00 | 2024-06-21 | |
| Aaron | AR0018PR-1g |
1-Naphthaleneethanamine, 7-methoxy- |
138113-09-4 | 95% | 1g |
$439.00 | 2025-02-11 | |
| eNovation Chemicals LLC | D212331-2.5g |
2-(7-Methoxynaphthalen-1-yl)ethanamine |
138113-09-4 | 95% | 2.5g |
$1480 | 2025-02-20 | |
| eNovation Chemicals LLC | D212331-5g |
2-(7-Methoxynaphthalen-1-yl)ethanamine |
138113-09-4 | 95% | 5g |
$1950 | 2025-02-20 | |
| eNovation Chemicals LLC | D212331-10g |
2-(7-Methoxynaphthalen-1-yl)ethanamine |
138113-09-4 | 95% | 10g |
$2860 | 2025-02-20 |
2-(7-methoxynaphthalen-1-yl)ethan-1-amine Suppliers
2-(7-methoxynaphthalen-1-yl)ethan-1-amine Related Literature
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Daniel Messmer,Stefan Salentinig,Jakob Heier Nanoscale, 2019,11, 6929-6938
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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Dan Yang,Yanping Zhou,Xianhong Rui,Jixin Zhu,Ziyang Lu,Eileen Fong,Qingyu Yan RSC Adv., 2013,3, 14960-14962
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
Additional information on 2-(7-methoxynaphthalen-1-yl)ethan-1-amine
Comprehensive Overview of 2-(7-Methoxynaphthalen-1-yl)ethan-1-amine (CAS No. 138113-09-4): Properties, Applications, and Research Insights
2-(7-Methoxynaphthalen-1-yl)ethan-1-amine, identified by its CAS number 138113-09-4, is a specialized organic compound with a unique structural framework combining a naphthalene core with an ethanamine side chain. This molecule has garnered significant attention in pharmaceutical and material science research due to its versatile chemical properties. The presence of a methoxy group at the 7-position of the naphthalene ring enhances its electron-donating characteristics, making it a valuable intermediate in synthetic chemistry.
Recent studies highlight the compound's potential in drug discovery, particularly in targeting G-protein-coupled receptors (GPCRs), a hot topic in neuropharmacology. Researchers are exploring its derivatives for modulating neurotransmitter activity, aligning with the growing demand for central nervous system (CNS) therapeutics. Its structural similarity to bioactive molecules like serotonin analogs further fuels interest in its structure-activity relationships (SAR).
From a synthetic chemistry perspective, CAS 138113-09-4 serves as a precursor for fluorescent probes, leveraging its naphthalene-based chromophore properties. This application resonates with the surge in bioimaging technologies, addressing frequent search queries like "naphthalene derivatives for cell imaging." The compound's photostability and tunable emission profiles make it suitable for live-cell tracking, a trending focus in cancer research.
Environmental and green chemistry applications are also emerging. The methoxy group’s influence on biodegradability positions this compound as a candidate for eco-friendly catalysts, responding to searches on "sustainable amine-based catalysts." Computational studies (molecular docking and DFT calculations) frequently cite its optimized electronic configuration, catering to AI-driven research trends.
In material science, 2-(7-methoxynaphthalen-1-yl)ethan-1-amine contributes to organic semiconductors and conductive polymers, aligning with queries like "amine-functionalized naphthalenes for OLEDs." Its charge transport efficiency and thermal stability are under investigation for next-gen flexible electronics, a sector experiencing exponential growth.
Quality control protocols for CAS 138113-09-4 emphasize HPLC purity analysis and spectroscopic characterization (NMR, MS), addressing lab technicians' searches for "standardized amine compound testing." Regulatory compliance focuses on REACH and ISO certification, ensuring safe handling without hazardous classifications.
Future directions include exploring its catalytic asymmetric synthesis potential and nanocarrier functionalization for drug delivery, topics frequently discussed in peer-reviewed journals. The compound’s adaptability across disciplines underscores its relevance in contemporary scientific discourse.
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