- 5-Aminoisoindolin-1-one
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- $1.10 / 1g
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2025-11-18
- CAS:222036-66-0
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons
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| | 5-Aminoisoindolin-1-one Basic information |
| Product Name: | 5-Aminoisoindolin-1-one | | Synonyms: | 1H-Isoindol-1-one,5-amino-2,3-dihydro-(9CI);5-amino-2,3-dihydro-1H-Isoindol-1-one;5-aminoisoindolin-1-one;1H-Isoindol-1-one, 5-amino-2,3-dihydro;5-aMino-2,3-dihydro- Isoindol-1-one;5-aMinoisoindoline-1-one;5-Aminoisoindolin-1-one ISO 9001：2015 REACH | | CAS: | 222036-66-0 | | MF: | C8H8N2O | | MW: | 148.16 | | EINECS: | 1592732-453-0 | | Product Categories: | Quinolines;AMINEPRIMARY | | Mol File: | 222036-66-0.mol |  |
| | 5-Aminoisoindolin-1-one Chemical Properties |
| Melting point | 197-199 °C(Solv: ethyl acetate (141-78-6)) | | Boiling point | 520.0±50.0 °C(Predicted) | | density | 1.307±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | form | solid | | pka | 15.12±0.20(Predicted) | | color | Yellow | | InChI | InChI=1S/C8H8N2O/c9-6-1-2-7-5(3-6)4-10-8(7)11/h1-3H,4,9H2,(H,10,11) | | InChIKey | RGJCJWXNNDARPQ-UHFFFAOYSA-N | | SMILES | C1(=O)C2=C(C=C(N)C=C2)CN1 |
| | 5-Aminoisoindolin-1-one Usage And Synthesis |
| Uses | 5-Aminoisoindolin-1-one is used in the synthesis of a novel potent glycoprotein IIb-IIIa (GP IIb-IIIa) receptor antagonist based on the isoindolone skeleton. | | Synthesis | General procedure for the synthesis of 5-amino-2,3-dihydroisoindol-1-one from 6-nitro-isoindolin-1-one: A mixture of 6-nitro-isoindolin-1-one (100 mg, 0.56 mmol), and reduced iron powder (314 mg, 5.6 mmol) was added to ethanol (2.0 mL) and concentrated hydrochloric acid (0.5 mL) and heated and refluxed for 2 hours. The completion of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, it was cooled to room temperature, the acid in the reaction solution was neutralized with a methanol solution saturated with ammonia (NH3), filtered through diatomaceous earth, the filtrates were washed with methanol, the filtrates were combined and the solvent was evaporated under reduced pressure to give 5-amino-2,3-dihydroisoindol-1-one (70.0 mg, 84% yield) as a white solid. | | References | [1] Patent: CN103804358, 2016, B. Location in patent: Paragraph 0126
[2] Patent: WO2012/92880, 2012, A1. Location in patent: Page/Page column 57
[3] Patent: US9138427, 2015, B2. Location in patent: Page/Page column 287
[4] Patent: WO2006/17443, 2006, A2. Location in patent: Page/Page column 154-155
[5] Patent: US2010/15141, 2010, A1. Location in patent: Page/Page column 26 |
| | 5-Aminoisoindolin-1-one Preparation Products And Raw materials |
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