(2E,4E)-5-(4-methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,4-dienal
(2E,4E)-5-(4-methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,4-dienal Basic information
- Product Name:
- (2E,4E)-5-(4-methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,4-dienal
- Synonyms:
-
- (2E,4E)-5-(4-methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,4-dienal
- Acitretin Impurity 3
- 2,4-Pentadienal, 5-(4-methoxy-2,3,6-trimethylphenyl)-3-methyl-, (2E,4E)-
- (2E,4E)-5-(4-Methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,...
- (2E,?4E)?-5-?(4-methoxy-?2,?3,?6-trimethylphenyl)?-?3-?methyl-2,?4-pentadienal
- CAS:
- 69877-38-9
- MF:
- C16H20O2
- MW:
- 244.33
- Mol File:
- 69877-38-9.mol
(2E,4E)-5-(4-methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,4-dienal Chemical Properties
- Density
- 1.003
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
(2E,4E)-5-(4-methoxy-2,3,6-trimethylphenyl)-3-methylpenta-2,4-dienal Usage And Synthesis
Synthesis
63650-98-6
69877-38-9
GENERAL METHOD: Sodium carbonate (4.77 g, 45 mmol) and activated manganese dioxide powder (3.91 g, 45 mmol) were added to a vigorously stirred solution of alcohols 27-31 (2.2 mmol) in dichloromethane (45 mL). The resulting suspension was stirred at room temperature until the reaction was complete (monitored by thin layer chromatography) and subsequently filtered through a diatomaceous earth pad. The filtrate was evaporated to dryness to obtain the residue. The residue was purified by fast column chromatography to afford allyl aldehydes 32-36 (only the 2E,4E-isomer was plotted).
References
[1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 2, p. 721 - 737
[2] Chemistry - A European Journal, 2014, vol. 20, # 29, p. 8904 - 8908
[3] Patent: US4169100, 1979, A
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