Basic information Safety Supplier Related

4-AMINO-N-METHYLPHTHALIMIDE

Basic information Safety Supplier Related

4-AMINO-N-METHYLPHTHALIMIDE Basic information

Product Name:
4-AMINO-N-METHYLPHTHALIMIDE
Synonyms:
  • N-METHYL-4-AMINO-PHTHALIMIDE
  • 5-amino-2-methyl-2,3-dihydro-1H-isoindole-1,3-dione
  • IFLAB-BB F1386-0358
  • 5-AMINO-2-METHYL-1H-ISOINDOLE-1,3(2H)-DIONE
  • 4-AMINO-N-METHYLPHTHALIMIDE
  • AKOS BBS-00002874
  • 4-Amino-N-methylphthalimide 97%
  • 4-Amino-N-methylphthalimide
CAS:
2307-00-8
MF:
C9H8N2O2
MW:
176.17
Product Categories:
  • N-Substituted Maleimides, Succinimides & Phthalimides
  • N-Substituted Phthalimides
  • Carbonyl Compounds
  • Cyclic Imides
  • Organic Building Blocks
Mol File:
2307-00-8.mol
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4-AMINO-N-METHYLPHTHALIMIDE Chemical Properties

Melting point:
246-248 °C(lit.)
Boiling point:
368.3±25.0 °C(Predicted)
Density 
1.411±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-0.27±0.20(Predicted)
Appearance
Light yellow to yellow Solid
CAS DataBase Reference
2307-00-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HS Code 
29251900

MSDS

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4-AMINO-N-METHYLPHTHALIMIDE Usage And Synthesis

General Description

The intermediate charge-transfer transients of 4-amino-N-methylphthalimide (4AMP) has been characterized by laser flash photolysis, steady-state and time-resolved fluorescence studies. 4AMP is a solvatochromic fluorescent dye. Transient solvation of 4AMP in binary supercritical fluids composed of 2-propanol and CO2 has been studied by frequency-domain fluorescence spectroscopy.

Synthesis

3676-85-5

74-88-4

2307-00-8

GENERAL STEPS: Potassium hydroxide (0.35 g, 6.17 mmol) was added to a solution of 4-amino-phthalimide (1.00 g, 6.17 mmol) in dimethylformamide (30 mL) and the reaction mixture was stirred at room temperature for 2 hours. Subsequently, iodomethane (0.88 g, 6.17 mmol) was added and stirring was continued at the same temperature for 18 hours. Upon completion of the reaction, water (50 mL) and ethyl acetate (50 mL) were added for extraction and the organic phase was separated. The organic phase was washed sequentially with saturated saline, dried with anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography (elution gradient: 0-100% cyclohexane solution of ethyl acetate) to afford N-methyl-4-amino phthalimide as a yellow solid (1.00 g, 92% yield). The product was characterized as follows: 1H NMR (DMSO-d6) δ 7.46 (d, J = 8.24 Hz, 1H), 6.90 (d, J = 2.00 Hz, 1H), 6.77 (dd, J = 8.24, 2.00 Hz, 1H), 6.42 (br.s, 2H), 2.94 (s, 3H); 13C NMR (DMSO-d6) δ 168.87, 168.57, 155.27, 135.10, 125.17, 117.33, 116.84, 107.42, 23.83; MS (m/z): 177 [M + H]+.

References

[1] Molecules, 2017, vol. 22, # 9,

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