3,5-Dimethoxybenzaldehyde, 98%
3,5-Dimethoxybenzaldehyde, 98%
3,5-Dimethoxybenzaldehyde, 98%
Thermo Scientific Chemicals

3,5-Dimethoxybenzaldehyde, 98%

CAS: 7311-34-4 | C9H10O3 | 166.18 g/mol
Quantity:
5 g
25 g
100 g
Catalog number A15109.14
also known as A15109-14
Price (JPY)
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Quantity:
25 g
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Chemical Identifiers
CAS7311-34-4
IUPAC Name3,5-dimethoxybenzaldehyde
Molecular FormulaC9H10O3
InChI KeyVFZRZRDOXPRTSC-UHFFFAOYSA-N
SMILESCOC1=CC(C=O)=CC(OC)=C1
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SpecificationsSpecification SheetSpecification Sheet
FormPowder or crystalline solid
Assay (GC)≥97.5%
Free acid (titration)<1.0%
Melting Point (clear melt)44-49?C
Appearance (Color)White to cream or pale yellow
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3,5-Dimethoxybenzaldehyde is used as a building block in organic synthesis. It is used to prepare isomeric hyperbranched polyetherketones.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3,5-Dimethoxybenzaldehyde is used as a building block in organic synthesis. It is used to prepare isomeric hyperbranched polyetherketones.

Solubility
Soluble in hot methanol. Insoluble in water.

Notes
Air sensitive. Incompatible with strong oxidizing agents, strong bases and strong reducing agents.
RUO – Research Use Only

General References:

  1. Masuoka, N.; Nihei, K. I.; Maeta, A.; Yamagiwa, Y.; Kubo, I. Inhibitory effects of cardols and related compounds on superoxide anion generation by xanthine oxidase. Food Chem. 2015, 166, 270-274.
  2. Khan, R.; Idris, M.; Tuncel, D. Synthesis and investigation of singlet oxygen production efficiency of photosensitizers based on meso-phenyl-2,5-thienylene linked porphyrin oligomers and polymers. Org. Biomol. Chem. 2015, 13 (42), 10496-10504.