Weight | 138.122 g/mol |
---|---|
Formula | C7H6O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3,5-Dihydroxybenzaldehyde (26153-38-8)
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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)
- Photo-protection by 3-bromo-4, 5-dihydroxybenzaldehyde against ultraviolet B-induced oxidative stress in human keratinocytes. (Ecotoxicology and Environmental Safety, 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)
- [Studies on antiseptics for foodstuff. 73. Studies on 3-halogeno-4-hydroxy-benzoic acid esters, 4-alkylresorcinol,4-arylresorcinol, 5-alkyl-2,4-dihydroxybenzaldehyde, 5-alkyl-3-chloro-2,4-dihydroxybenzaldehyde, 4-aryl-6-chlororesorcinol and phenylaminothioformic acid esters as a preservative for sake]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1972)
- New Schiff bases derived from 2,5-dihydroxybenzaldehyde and amino-substituted 2-phenyl-1,3-benzothiazoles. Mesogenic monomers for liquid crystalline polyethers (Russian Journal of Organic Chemistry, 2011)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C=C(C=C1O)O)C=O
-
InChIKeyHAQLHRYUDBKTJG-UHFFFAOYSA-N
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