2,5-Dimethoxybenzaldehyde, 98+%
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 NumberQuantity
ALFA19928.1425 g
Catalog number ALFA19928.14
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25 g
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Specifications
Chemical Name or Material2,5-Dimethoxybenzaldehyde
CAS93-02-7
Health Hazard 1H315-H319-H335
Health Hazard 2GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P270-P271-P280-P285-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P342+P311-P362-P501c
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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.