Basic information Uses Safety Supplier Related

2 4-DIHYDROXY-6-METHYLBENZALDEHYDE

Basic information Uses Safety Supplier Related

2 4-DIHYDROXY-6-METHYLBENZALDEHYDE Basic information

Product Name:
2 4-DIHYDROXY-6-METHYLBENZALDEHYDE
Synonyms:
  • 133345
  • Orcylaldehyde
  • Orcylic aldehyde
  • 2,4-Dihydroxy-6-methylbenzaldehyde
  • 6-Methyl-β-resorcyladehyde
  • Benzaldehyde, 2,4-dihydroxy-6-methyl-
  • 2,4-Dihydroxy-6-Methylbenz
  • 2,4-Dihydroxy-6-methylbenzaldehyde - [D71751]
CAS:
487-69-4
MF:
C8H8O3
MW:
152.15
Product Categories:
  • C8
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • Aldehydes
  • Building Blocks
Mol File:
487-69-4.mol
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2 4-DIHYDROXY-6-METHYLBENZALDEHYDE Chemical Properties

Melting point:
180-184 °C
Boiling point:
321.9±22.0 °C(Predicted)
Density 
1.331±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
DMSO (Sparingly), Methanol (Slightly)
form 
crystalline needles
pka
7.69±0.23(Predicted)
color 
Burnt orange
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38-43
Safety Statements 
26-36/37
WGK Germany 
3
HS Code 
2912490090
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2 4-DIHYDROXY-6-METHYLBENZALDEHYDE Usage And Synthesis

Uses

2,4-Dihydroxy-6-methylbenzaldehyde is mainly used in pharmaceuticals and experimental research.

Definition

ChEBI: 2,4-dihydroxy-6-methylbenzaldehyde is a dihydroxybenzaldehyde that is 2,4-dihydroxybenzaldehyde in which the hydrogen at position 6 has been replaced by a methyl group. It is a fungal metabolite isolated from Grifola frondosa and Phlebiopsis gigantea. It has a role as an apoptosis inducer, an anti-inflammatory agent and a fungal metabolite.

Synthesis

504-15-4

68-12-2

487-69-4

5-Methylbenzene-1,3-diol (25.0 g, 0.2 mol) was dissolved in N,N-dimethylformamide (100 mL) at 0 °C and slowly added dropwise to a pre-cooled mixture of POCl3 (44.0 g, 0.3 mol) and N,N-dimethylformamide (200 mL). After the dropwise addition was completed, the reaction mixture was stirred at room temperature for 1 hour. Subsequently, the reaction mixture was slowly poured into ice water and the solid product was precipitated. The solid was collected by filtration and washed three times with distilled water to remove residual acid and solvent. Finally, the product was dried to afford 2,4-dihydroxy-6-methylbenzaldehyde (21.0 g, 82.0% yield), which could be used in subsequent reactions without further purification.

References

[1] Organic Letters, 2003, vol. 5, # 23, p. 4481 - 4484
[2] Patent: WO2004/58738, 2004, A1. Location in patent: Page 2/2; 10
[3] Journal of Medicinal Chemistry, 2001, vol. 44, # 5, p. 664 - 671
[4] Patent: WO2017/151489, 2017, A1. Location in patent: Paragraph 0284
[5] Molecules, 2018, vol. 23, # 10,

2 4-DIHYDROXY-6-METHYLBENZALDEHYDESupplier

Xiamen Work-For-World Medcine Co., Ltd Gold
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18622448868
Email
jpjchem@163.com
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2 4-DIHYDROXY-6-METHYLBENZALDEHYDE(487-69-4)Related Product Information