Weight | 138.122 g/mol |
---|---|
Formula | C7H6O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
2,3-Dihydroxybenzaldehyde (24677-78-9)
o-pyrocatechualdehyde
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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)
- Preconcentration of Heavy Metals and Matrix Elimination using Silica Gel Chemically Modified with 2,3Dihydroxybenzaldehyde (Separation Science and Technology, 2007)
- Investigation of the Electromethoxylation Reaction Part 2: Electrochemical Study of 3-Methylcatechol and 2,3-Dihydroxybenzaldehyde in Methanol (Electroanalysis, 2001)
- ELECTROCHEMICAL STUDY OF 2,3-DIHYDROXYBENZALDEHYDE IN THE PRESENCE OF 4-HYDROXYCOUMARIN APPLICATION TO THE ELECTRO-ORGANIC SYNTHESIS OF NEW COUMESTAN DERIVATIVE (Bulletin of Electrochemistry, 1998)
- Palladium salicylaldimine complexes derived from 2,3-dihydroxybenzaldehyde (Inorganica Chimica Acta, 2011)
- Synthesis of Hydroxybenzaldehyde Stable Phosphorus Ylides from the Reaction Between Acetylenic Esters with Triphenylphosphine in the Presence of 2,3-Dihydroxybenzaldehyde and 2-Hydroxy-4-methoxybenzaldehyde (Phosphorus Sulfur and Silicon and The Related Elements, 2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o-pyrocatechualdehyde
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SMILESC1=CC(=C(C(=C1)O)O)C=O
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InChIKeyIXWOUPGDGMCKGT-UHFFFAOYSA-N
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