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ISOQUINOLINE-5-CARBOXYLIC ACID

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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
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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)
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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
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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

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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