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| | ISOQUINOLINE-5-CARBOXYLIC ACID Basic information |
| | ISOQUINOLINE-5-CARBOXYLIC ACID Chemical Properties |
| Melting point | 278-281°C | | Boiling point | 60-62°C 11mm | | density | 1.339±0.06 g/cm3(Predicted) | | Fp | 60-62°C/11mm | | storage temp. | 2-8°C(protect from light) | | pka | 1.21±0.10(Predicted) | | form | solid | | Appearance | White to off-white Solid | | BRN | 129180 | | InChI | 1S/C10H7NO2/c12-10(13)9-3-1-2-7-6-11-5-4-8(7)9/h1-6H,(H,12,13) | | InChIKey | ZIPLFLRGHZAXSJ-UHFFFAOYSA-N | | SMILES | OC(=O)c1cccc2cnccc12 | | CAS DataBase Reference | 27810-64-6(CAS DataBase Reference) |
| Hazard Codes | Xn | | Risk Statements | 36/37/38-36-22 | | Safety Statements | 26-36/37/39-22 | | WGK Germany | 3 | | HS Code | 2933499090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral
Eye Irrit. 2 |
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| | ISOQUINOLINE-5-CARBOXYLIC ACID Usage And Synthesis |
| Uses | Isoquinoline-5-carboxylic acid is an isoquinoline derivative. This group of substances can be used as raw materials for organic synthesis in the preparation of other heterocyclic compounds or pharmaceutical products. Studies have shown that its derivative isoquinoline-3-carboxylic acid (IQ3CA) has antimicrobial activity and is a lead compound with antimicrobial properties for plant diseases[1]. | | Synthesis | The general procedure for the synthesis of isoquinoline-5-carboxylic acid from 5-cyanoisoquinoline was as follows: isoquinoline-5-carbonitrile (6 g, 38.62 mmol) prepared in step (1) was mixed with distilled water (90 mL) and stirred until homogeneous. Concentrated hydrochloric acid solution (15 mL) was slowly added to the reaction system, followed by heating the reaction mixture to 100 °C and continuous stirring for 6 hours. Upon completion of the reaction, the mixture was cooled to room temperature and the pH was adjusted to 5~6 by dropwise addition of N,N-diisopropylethylamine (DIPEA, ca. 40 mL).The resulting suspension was continued to be stirred at room temperature for 3 hr, followed by diafiltration. The collected solid product was dried in an oven at 50 °C to give final isoquinoline-5-carboxylic acid (5.6 g, 84% yield). Mass spectrum (ESI+, m/z): 174 [M+H]+. | | References | [1] XU Z, DING H, XIN F, et al. Antibacterial Activity and Possibly Made of Action of Isoquinoline-3-Carboxylic Acid[J]. Natural Product Communications, 2024. DOI:10.1177/1934578x241226562. |
| | ISOQUINOLINE-5-CARBOXYLIC ACID Preparation Products And Raw materials |
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