CARBOSTYRIL 124
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
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)
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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