Basic information Safety Supplier Related

9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine

Basic information Safety Supplier Related

9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine Basic information

Product Name:
9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine
Synonyms:
  • 8-Hydroxy-1,1,7,7-tetramethyl-1,2,3,5,6,7-hexahydro-pyrido[3,2,1-ij]quinoline-9-carbaldehyde
  • 9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine
  • 8-HYDROXY-1,1,7,7-TETRAMETHYL-2,3,6,7-TETRAHYDRO-1H,5H-PYRIDO[3,2,1-IJ]QUINOLINE-9-CARBOXALDEHYDE
  • 8-HYDROXY-1,1,7,7-TETRAMETHYLJULOLIDINE-9-CARBOXALDEHYDE
  • 8-HYDROXY-1,1,7,7-TETRAMETHYLJULOLIDINE-9-CARBOXALDEHYDE 99%
  • 8-Hydroxy-1,1,7,7-tetramethyljulolidine-9-carboxaldehyde,99%
  • 1,1,7,7-Tetramethyl-8-hydroxy-9-formyljulolidine
  • 9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine 2,3,6,7-Tetrahydro-8-hydroxy-1,1,7,7-tetramethyl-1H,5H-benzo[ij]quinolizine-9-carboxaldehyde
CAS:
115662-09-4
MF:
C17H23NO2
MW:
273.37
Product Categories:
  • Quinoline&Isoquinoline
Mol File:
115662-09-4.mol
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9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine Chemical Properties

Melting point:
74-77 °C
Boiling point:
416.39°C (rough estimate)
Density 
1.0101 (rough estimate)
refractive index 
1.5200 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
soluble in Methanol
form 
powder to crystal
pka
9.50±0.60(Predicted)
color 
White to Light yellow to Green
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Safety Information

Safety Statements 
24/25
HS Code 
29339900

MSDS

  • Language:English Provider:ACROS
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9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine Usage And Synthesis

Chemical Properties

Light Green Crystals

Synthesis

115704-83-1

68-12-2

115662-09-4

GENERAL METHODS: 8-Hydroxy-1,1,7,7-tetramethyl-2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinoline-8-ol and N,N-dimethylformamide were used as raw materials to synthesize 8-hydroxy-1,1,7,7-tetramethyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline-9-carbaldehyde. The procedure was as follows: to a magnetically stirred solution of N,N-dimethylformamide (2 mL, 23 mmol) of phosphorous trichloride (2.2 mL, 23 mmol) under argon protection, 1,1,7,7-tetramethyl-2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-8-aldehyde (2 g, 11.6 mmol) was slowly added at 0°C and additional of N,N-dimethylformamide (2 mL). Subsequently, the reaction mixture was stirred at room temperature for 3 h and the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was neutralized with ammonium hydroxide solution and then the product was extracted with ethyl acetate. The organic phase was washed several times with water to remove impurities. Finally, the residue was purified by column chromatography (silica gel as stationary phase and 10% ethyl acetate/hexane as eluent) to afford the target product 8-hydroxy-1,1,7,7-tetramethyl-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinoline-9-carboxaldehyde in a yield of 1.8 g (80% yield).

References

[1] Molecular Crystals and Liquid Crystals, 2008, vol. 491, p. 152 - 163
[2] Tetrahedron Letters, 2018, vol. 59, # 29, p. 2788 - 2792

9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidine Preparation Products And Raw materials

Raw materials

9-Formyl-8-hydroxy-1,1,7,7-tetramethyljulolidineSupplier

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