ISOQUINOLINE-5-CARBOXYLIC ACID
ISOQUINOLINE-5-CARBOXYLIC ACID Basic information
- Product Name:
- ISOQUINOLINE-5-CARBOXYLIC ACID
- Synonyms:
-
- RARECHEM AL BE 1523
- ISOQUINOLINE-5-CARBOXYLIC ACID
- Isoquinoline-5-carboxylicacid,96%
- 5-isoquinolinecarboxylic acid
- 5-Carboxyisoquinoline
- 5-Carboxyisoquinoline, 2-Azanaphthalene-5-carboxylic acid
- ine-5-carboxyL
- 5-Isoquinolinecarboxylicaci
- CAS:
- 27810-64-6
- MF:
- C10H7NO2
- MW:
- 173.17
- EINECS:
- 640-129-5
- Product Categories:
-
- Acids and Derivatives
- Heterocycles
- Building Blocks
- Isoquinoline
- Isoquinoline Derivertives
- Mol File:
- 27810-64-6.mol
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)
- Flash point:
- 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
- CAS DataBase Reference
- 27810-64-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 36/37/38-36-22
- Safety Statements
- 26-36/37/39-22
- WGK Germany
- 3
- HS Code
- 2933499090
MSDS
- Language:English Provider:ALFA
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
27655-41-0
27810-64-6
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.
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ISOQUINOLINE-5-CARBOXYLIC ACID(27810-64-6)Related Product Information
- 6-isoquinolinecarboxylic acid
- 7-isoquinolinecarboxylic acid
- ISOQUINOLINE-8-CARBALDEHYDE
- 5-CYANOISOQUINOLINE
- 1-ISOQUINOLINEMETHANOL
- POTASSIUM ISOQUINOLINE-4-TRIFLUOROBORATE
- ISOQUINOLINE-1-CARBOXYLIC ACID
- ISOQUINOLINE-3-CARBOXYLIC ACID
- ISOQUINOLINE-3-CARBOXYLIC ACID METHYL ESTER
- 6-Isoquinolinecarboxaldehyde (9CI)
- Isoquinoline-4-carbaldehyde
- 6-Isoquinolinyl-boronic acid
- 8-isoquinolinyl-boronic acid
- C-ISOQUINOLIN-4-YL-METHYLAMINE
- 7-Isoquinolinecarboxaldehyde (6CI,9CI)
- ISOQUINOLINE-5-CARBALDEHYDE
- 3-isoquinolinecarboxaldehyde
- ISOQUINOLINE N-OXIDE