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CARBOSTYRIL 124

Basic information Safety Supplier Related

CARBOSTYRIL 124 Basic information

Product Name:
CARBOSTYRIL 124
Synonyms:
  • 7-amino-4-methyl-2(1h)-quinolinon
  • 7-AMINO-4-METHYL-2(1H)-QUINOLINONE
  • 7-AMINO-2-HYDROXY-4-METHYLQUINOLINE
  • CARBOSTYRIL 7
  • CARBOSTYRIL 124
  • 7-amino-4-methyl-2-quinolone
  • CARBOSTYRIL 124 99%
  • 7-amino-4-methylquinolin-2(1H)-one
CAS:
19840-99-4
MF:
C10H10N2O
MW:
174.2
EINECS:
243-363-2
Product Categories:
  • Quinolines, Quinazolines and derivatives
  • Chemical Amines
  • Amines
  • Aromatics
  • Heterocycles
Mol File:
19840-99-4.mol
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CARBOSTYRIL 124 Chemical Properties

Melting point:
>275°C (dec.)
Boiling point:
417.6±45.0 °C(Predicted)
Density 
1.223±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
11.45±0.70(Predicted)
color 
Off-White to Light Beige
Appearance
Off-white to light beige solid
λmax
350 nm
EPA Substance Registry System
2(1H)-Quinolinone, 7-amino-4-methyl- (19840-99-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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CARBOSTYRIL 124 Usage And Synthesis

Description

Suitable as a laser dye. Dyes and metabolites.

Chemical Properties

Off-White to Tan Solid

Uses

Suitable as a laser dye

General Description

Carbostyril 124 (CS124) is a chromophore that can be used as a laser dye for sensitization and optical detection. It acts as an antenna molecule that facilitates the light absorption and enhances fluorescence efficiency.

Synthesis

141-97-9

108-45-2

19840-99-4

GENERAL PROCEDURE: Isophthalamide (1.0 g, 9.3 mmol) was added to ethyl acetoacetate (1.2 eq, 2-3.6 g) and the mixture was heated to reflux for 20 hours. After completion of the reaction, the mixture was poured into ice (100 g) and the precipitate was collected by filtration. Purification by silica gel column chromatography (100-200 mesh, eluent methanol/chloroform, 1:99 v/v) afforded 7-amino-4-methylquinolin-2(1H)-one.

References

[1] Medicinal Chemistry Research, 2013, vol. 22, # 11, p. 5227 - 5235
[2] Medicinal Chemistry Research, 2010, vol. 19, # 2, p. 193 - 209
[3] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 4, p. 1624 - 1638
[4] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 24, p. 8712 - 8728
[5] Journal of Medicinal Chemistry, 2016, vol. 59, # 4, p. 1648 - 1653

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