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2,4-Dimethoxybenzaldehyde is used as a reagent to specifically quantify phlorotannins. It is also used as a component of hair dyes.
Aliakbar Dehno Khalaji; Karla Fejfarova; Michal Dusek. Synthesis and characterization of two Diimine Schiff Bases derived from 2,4-dimethoxybenzaldehyde: The crystal structure of N,N-Bis(2,4-dimethoxybenzylidene)-1,2-diaminoethane. Acta Chim. Slov. 2010, 57, 257-261
Kou-Chang Liu; Becky R.Shelton; Robert K.Howe. A particularly convenient preparation of benzohydroximinoyl chlorides (nitrile oxide precursors). J. Org. Chem. 1980, 45, (19)3916-3918
Has been used to protect diols as their cyclic acetals, by azeotroping in the presence of TsOH: J. Am. Chem. Soc., 84, 430 (1962). The products are readily hydrolyzed by acid but are stable to hydrogenolysis conditions (Raney Ni) used to cleave O-benzyl groups: Tetrahedron, 42, 3021 (1986).
Gefahrenhinweise (EU): H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.