2,5-Dimethoxybenzaldehyde, 98+%
2,5-Dimethoxybenzaldehyde, 98+%
2,5-Dimethoxybenzaldehyde, 98+%
Thermo Scientific Chemicals

2,5-Dimethoxybenzaldehyde, 98+%

CAS: 93-02-7 | C9H10O3 | 166.176 g/mol
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Catalog number A19928.36
also known as A19928-36
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294,00
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Quantity:
500 g
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Price (EUR)
294,00
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Chemical Identifiers
CAS93-02-7
IUPAC Name2,5-dimethoxybenzaldehyde
Molecular FormulaC9H10O3
InChI KeyAFUKNJHPZAVHGQ-UHFFFAOYSA-N
SMILESCOC1=CC=C(OC)C(C=O)=C1
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder or chunks or flakes
Assay (GC)≥98.0%
Melting Point (clear melt)45.0-51.0?C
Appearance (Color)Pale cream to cream to yellow to pale brown
Free acid (titration)≤1%
2,5-Dimethoxybenzaldehyde is used in the preparation of 2,5-dimethoxyphenethylamine, which is utilized to prepare psychoactive drugs such as 2,5-dimethoxy-4-bromophenethylamine, 2,5-dimethoxy-4-iodophenethylamine and 4-Chloro-2,5-dimethoxy-phenethylamine. It acts as an intermediate in organic synthesis.

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
2,5-Dimethoxybenzaldehyde is used in the preparation of 2,5-dimethoxyphenethylamine, which is utilized to prepare psychoactive drugs such as 2,5-dimethoxy-4-bromophenethylamine, 2,5-dimethoxy-4-iodophenethylamine and 4-Chloro-2,5-dimethoxy-phenethylamine. It acts as an intermediate in organic synthesis.

Solubility
Soluble in chloroform and methanol. Slightly soluble in water.

Notes
Air sensitive. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Zolfigol, M. A.; Baghery, S.; Moosavi-Zare, A. R.; Vahdat, S. M.; Alinezhad, H.; Norouzi, M. Design of 1-methylimidazolium tricyanomethanide as the first nanostructured molten salt and its catalytic application in the condensation reaction of various aromatic aldehydes, amides and beta-naphthol compared with tin dioxide nanoparticles. RSC Adv. 2015, 5 (56), 45027-45037.
  2. Prakash, K. S.; Nagarajan, R. Total synthesis of the marine alkaloids Caulibugulones A and D. J. Anal. Appl. Pyrolysis 2015, 71 (5), 801-804.