4-Bromo-2,5-dimethoxybenzaldehyde

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Products Intro: Product Name:4-Bromo-2,5-dimethoxybenzaldehyde
CAS:31558-41-5
Purity:99% Package:1KG;10.00;USD
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Products Intro: Product Name:4-Bromo-2, 5-Dimethoxybenzaldehyde
CAS:31558-41-5
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Products Intro: Product Name:4-Bromo-2,5-dimethoxybenzaldehyde
CAS:31558-41-5
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Products Intro: Product Name:4-Bromo-2,5-dimethoxybenzaldehyde
CAS:31558-41-5
Purity:99% Package:1KG;1USD
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Products Intro: Product Name:4-Bromo-2,5-dimethoxybenzaldehyde
CAS:31558-41-5
Purity:0.99 Package:100g, 500g, 1kg, 25kg, 50kg, 200kg Remarks:Good quality; Large stock; Hot sale

4-Bromo-2,5-dimethoxybenzaldehyde manufacturers

4-Bromo-2,5-dimethoxybenzaldehyde Basic information
Product Name:4-Bromo-2,5-dimethoxybenzaldehyde
Synonyms:4-Bromo-2,5-dimethoxybenzaldehyde, 98+%;4-bromo-2,5-dimethoxybenzaldehyde(SALTDATA: FREE);4-Bromo-2,5-dimethoxybenzaldehyde 98%;Benzaldehyde, 4-bromo-2,5-dimethoxy-;4-Bromo-2,5-dimethoxybenzaldehyde ISO 9001:2015 REACH
CAS:31558-41-5
MF:C9H9BrO3
MW:245.07
EINECS:
Product Categories:
Mol File:31558-41-5.mol
4-Bromo-2,5-dimethoxybenzaldehyde Structure
4-Bromo-2,5-dimethoxybenzaldehyde Chemical Properties
Melting point 132-135°C
Boiling point 337.1±42.0 °C(Predicted)
density 1.482±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form solid
color Faint yellow to yellow
Water Solubility Insoluble in water.
Stability:Hygroscopic
InChIInChI=1S/C9H9BrO3/c1-12-8-4-7(10)9(13-2)3-6(8)5-11/h3-5H,1-2H3
InChIKeyBIFWGDWGCZLCHF-UHFFFAOYSA-N
SMILESC(=O)C1=CC(OC)=C(Br)C=C1OC
Safety Information
HS Code 2913000090
MSDS Information
4-Bromo-2,5-dimethoxybenzaldehyde Usage And Synthesis
Uses4-Bromo-2,5-dimethoxybenzene is used as a pharmaceutical intermediate.
Synthesis
2,5-Dimethoxybenzaldehyde

93-02-7

4-Bromo-2,5-dimethoxybenzaldehyde

31558-41-5

At 0 °C, 2,5-dimethoxybenzaldehyde (1.0 g, 6.02 mmol) was dissolved in glacial acetic acid (7 mL) and a solution of bromine (0.34 mL, 6.62 mmol) in glacial acetic acid (3 mL) was slowly added. The reaction mixture was gradually warmed to room temperature and stirred continuously for 1 hour. Upon completion of the reaction, water (30 mL) was added to quench the reaction and the resulting white precipitate was collected by filtration. The precipitate was redissolved in water (30 mL) and dichloromethane (30 mL) for liquid-liquid separation. The aqueous phase was extracted with dichloromethane (3 x 25 mL), and all organic phases were combined, washed with brine (25 mL), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography (eluent: 20% ethyl acetate/hexane) to afford 4-bromo-2,5-dimethoxybenzaldehyde as a light yellow solid (0.83 g, 3.37 mmol, 56% yield).

References[1] Organic and Biomolecular Chemistry, 2013, vol. 11, # 35, p. 5782 - 5786
[2] Tetrahedron, 2011, vol. 67, # 21, p. 3904 - 3914
[3] Journal of the American Chemical Society, 2011, vol. 133, # 40, p. 15870 - 15873
[4] Synthetic Communications, 1998, vol. 28, # 24, p. 4629 - 4637
[5] Tetrahedron Letters, 2003, vol. 44, # 16, p. 3281 - 3284
Tag:4-Bromo-2,5-dimethoxybenzaldehyde(31558-41-5) Related Product Information
4-Bromo-2,5-dimethylbenzoic acid 4-Bromo-2,5-dimethylphenylboronic acid 4-BROMO-2,5-DIMETHOXY-PHENOL (4-BROMO-2,5-DIMETHOXYPHENYL)METHANOL 4-BROMO-2,5-DIMETHOXYBENZOIC ACID 4-Bromo-2-hydroxybenzaldehyde 2-Bromo-4-methoxybenzenol 5-Bromo-2-methylphenol 4-Bromo-2,5-dimethoxybenzaldehyde BROMOHYDROQUINONE 4-BROMO-2-METHOXYBENZALDEHYDE 1-Bromo-2,5-dimethoxybenzene 4-BROMO-2,5-DIMETHOXYTOLUENE 2,5-Dimethoxybenzaldehyde 4-BROMO-3-HYDROXYBENZALDEHYDE 2-BROMO-4-METHOXYPHENOL 4-BROMO-3-METHOXYPHENYL-P-TOLUENESULFONATE 4-BROMO-2-METHOXYTOLUENE