Basic information Safety Supplier Related

4-METHYLINDOLE-3-CARBOXALDEHYDE

Basic information Safety Supplier Related

4-METHYLINDOLE-3-CARBOXALDEHYDE Basic information

Product Name:
4-METHYLINDOLE-3-CARBOXALDEHYDE
Synonyms:
  • 4-Methylindole-3-caboxaldehyde
  • 1H-Indole-3-carboxaldehyde, 4-methyl- (9CI)
  • 4-methyl-1H-indole-3-carbaldehyde(SALTDATA: FREE)
  • 4-Methyl-1H-indole-3-carboxaldehyde
  • 4-Methyl-3-indolecarboxaldehyde
  • 1H-Indole-3-carboxaldehyde, 4-Methyl-
  • 4-Methyl-3-carboxaldehyde
  • 4-METHYLINDOLE-3-ALDEHYDE
CAS:
4771-48-6
MF:
C10H9NO
MW:
159.18
Product Categories:
  • ALDEHYDE
Mol File:
4771-48-6.mol
More
Less

4-METHYLINDOLE-3-CARBOXALDEHYDE Chemical Properties

Melting point:
192-194℃
Boiling point:
347.0±22.0 °C(Predicted)
Density 
1.226
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
15.86±0.30(Predicted)
Appearance
Yellow to brown Solid
More
Less

Safety Information

Risk Statements 
36
Safety Statements 
26
HazardClass 
IRRITANT
HS Code 
2933998090
More
Less

4-METHYLINDOLE-3-CARBOXALDEHYDE Usage And Synthesis

Synthesis

16096-32-5

68-12-2

4771-48-6

GENERAL STEPS: The Vilsmeier-Haack reagent was prepared by slowly adding POCl3 (60 mmol, 6 mL) dropwise to dry DMF (30 mL) pre-cooled to 0 °C under stirring conditions. Subsequently, the reaction mixture was continued to be stirred at 0 °C for 10-15 min. 4-Methylindole (10 mmol) was dissolved in DMF (5 mL) and the resulting solution was added within the Vilsmeier-Haack reagent prepared above. The reaction mixture was warmed to 35 °C with continuous stirring for 1 hour. After completion of the reaction, it was cooled to room temperature and ice water (6 mL) and 30% NaOH aqueous solution (13 mL) were added sequentially, followed by heating the mixture to reflux for 20 min and then cooled to room temperature. The reaction mixture was extracted with dichloromethane (20 mL x 3), the organic phases were combined and dried with anhydrous Na2SO4. The solvent was removed by concentration under reduced pressure and the resulting crude product was purified by fast column chromatography using 15-25% acetone/petroleum ether (boiling range 60-90 °C) as eluent to afford the target product 4-methylindole-3-carbaldehyde.

References

[1] Chemical Biology and Drug Design, 2011, vol. 78, # 5, p. 864 - 868
[2] European Journal of Medicinal Chemistry, 2015, vol. 92, p. 776 - 783
[3] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 7, p. 1301 - 1305
[4] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 6, p. 1793 - 1798
[5] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 7, p. 3780 - 3790

4-METHYLINDOLE-3-CARBOXALDEHYDE Preparation Products And Raw materials

Raw materials

4-METHYLINDOLE-3-CARBOXALDEHYDESupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Carbott PharmTech Inc.
Tel
0535-6385396
Email
info@carbottpharm.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com