| Weight | 138.122 g/mol |
|---|---|
| Formula | C7H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,5-Dihydroxybenzaldehyde (1194-98-5)
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- Synthesis and spectral studies of 5-[3-(1,2,4-triazolyl-azo]-2,4-dihydroxybenzaldehyde (TA) and its Schiff bases with 1,3-diaminopropane (TAAP) and 1,6-diaminohexane (TAAH). Their analytical application for spectrophotometric microdetermination of cobalt(II). Application in some radiochemical studies (Dyes and Pigments, 2005)
- A bioanode based on MWCNT/protein-assisted co-immobilization of glucose oxidase and 2,5-dihydroxybenzaldehyde for glucose fuel cells. (Biosensors and Bioelectronics, 2010)
- A three-dimensional porous metalorganic framework [Fe2L3(DMF)7(C4H10O)0.5] constructed from triple-helices {L = bis[2,4-dihydroxybenzaldehyde]hydrazone} (Journal of The Chemical Society-dalton Transactions, 2002)
- Sequential CN and CO 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)
- New organotin(IV) complexes with N(4)-methylthiosemicarbazone derivatives prepared from 2,3-dihydroxybenzaldehyde and 2-hydroxy-5-methylbenzaldehyde: synthesis, characterization, and cytotoxic activity (Journal of Coordination Chemistry, 2015)
- Mechanistic study of electrochemical oxidation of 2,5-dihydroxybenzoic acid and 3,4-dihydroxybenzaldehyde in the presence of 3-hydroxy-1H-phenalene-1-one. (Chemical & Pharmaceutical Bulletin, 2008)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CC(=C(C=C1O)C=O)O
-
InChIKeyCLFRCXCBWIQVRN-UHFFFAOYSA-N
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