- 7-Aminoquinoline
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- $1.10
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2026-08-20
- CAS:580-19-8
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons
- 7-Aminoquinoline
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2025-04-04
- CAS:580-19-8
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1Ton
- 7-Aminoquinoline
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- $1180.00
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2024-02-19
- CAS:580-19-8
- Min. Order: 1g
- Purity: 98
- Supply Ability: 500 Kg
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| | 7-Aminoquinoline Basic information |
| Product Name: | 7-Aminoquinoline | | Synonyms: | 7-QUINOLINAMINE;Quinolin-7-ylamine;7-quinolylamine;quinolin-7-amine(SALTDATA: FREE);7-Aminoquinoline;7-amine-quinoline;7-Quinolinamine (9CI);quinolin-7-amine acetate | | CAS: | 580-19-8 | | MF: | C9H8N2 | | MW: | 144.17 | | EINECS: | 811-260-7 | | Product Categories: | Quinoline Derivertives | | Mol File: | 580-19-8.mol |  |
| | 7-Aminoquinoline Chemical Properties |
| Melting point | 93.5-94 °C | | Boiling point | 324.3±15.0 °C(Predicted) | | density | 1.210±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | pka | 6.60±0.14(Predicted) | | form | powder to crystal | | color | White to Orange to Green | | InChI | InChI=1S/C9H8N2/c10-8-4-3-7-2-1-5-11-9(7)6-8/h1-6H,10H2 | | InChIKey | RZAUIOKDXQWSQE-UHFFFAOYSA-N | | SMILES | N1C2C(=CC=C(N)C=2)C=CC=1 | | CAS DataBase Reference | 580-19-8 | | NIST Chemistry Reference | 7-Quinolinamine(580-19-8) |
| WGK Germany | WGK 3 | | HS Code | 2933998090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2 |
| | 7-Aminoquinoline Usage And Synthesis |
| Uses | 7-Aminoquinoline Is an aminoquinolines derivative with antiviral activity. | | Synthesis | The general procedure for the synthesis of 7-aminoquinoline from 7-nitroquinoline is as follows: a reduction reaction is carried out according to the reaction conditions described in Scheme 14 to convert 7-nitroquinoline to 7-aminoquinoline. The specific operation involves adding a reducing agent (e.g., iron powder or hydrogen/Pd-C) in a suitable solvent and reacting under heating conditions until the reaction is complete. Upon completion of the reaction, the insoluble material is removed by filtration (e.g., reduction with iron powder) or the solvent is removed by distillation (e.g., reduction with hydrogen/Pd-C) to give the crude product. The crude product can be further purified by recrystallization or column chromatography to give pure 7-aminoquinoline. | | References | [1] Patent: US2006/194801, 2006, A1. Location in patent: Page/Page column 53
[2] Patent: US2006/205773, 2006, A1. Location in patent: Page/Page column 29
[3] Steroids, 1995, vol. 60, # 10, p. 693 - 698
[4] Patent: US9522908, 2016, B2. Location in patent: Paragraph 55; 59
[5] Journal of Medicinal Chemistry, 2007, vol. 50, # 15, p. 3497 - 3514 |
| | 7-Aminoquinoline Preparation Products And Raw materials |
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