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It is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff.
Chung-Mu Yu; Miao-Ju Yen; Lin-Chi Chen. A bioanode based on MWCNT/protein-assisted co-immobilization of glucose oxidase and 2,5-dihydroxybenzaldehyde for glucose fuel cells. Biosensors and Bioelectronics. 2010, 25 (11), 2515-2521.
Javed Iqbal; Neelima D Tangellamudi; Balakrishna Dulla; Sridhar Balasubramanian. Sequential C-N and C-O bond formation in a single pot: synthesis of 2H-benzo[b][1,4]oxazines from 2,5-dihydroxybenzaldehyde and amino acid precursors. Organic Letters. 2012, 14, (2), 552-555.
Has been converted conveniently in 4 steps to 4,7-dibenzyloxyindole via the Nenitzescu indole synthesis (Henry reaction with Nitromethane, A11806). The product is a precursor of pyrroloquinoline alkaloids: Synlett, 755 (1993).
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.