| Weight | 138.122 g/mol |
|---|---|
| Formula | C7H6O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3,4-Dihydroxybenzaldehyde (139-85-5)
protocatechuic aldehyde · protocatechualdehyde · rancinamycin IV
Score:
#1944 in Biochemistry
,
#5200 in Chemistry
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- Mechanistic Studies of the Electrocatalytic Oxidation of NADH and Ascorbate at Glassy Carbon Electrodes Modified with Electrodeposited Films Derived from 3,4-Dihydroxybenzaldehyde. (Analytical Chemistry, 1997)
- Electrocatalysis of NADH oxidation with electropolymerized films of 3,4-dihydroxybenzaldehyde (Analytical Chemistry, 1994)
- Protocatechuic aldehyde suppresses TNF--induced ICAM-1 and VCAM-1 expression in human umbilical vein endothelial cells (European Journal of Pharmacology, 2005)
- 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)
- Studies on the effect of vanillin and protocatechualdehyde on the corrosion of steel in hydrochloric acid (Materials Chemistry and Physics, 2004)
- Solid phase extraction using nanoporous MCM-41 modified with 3,4-dihydroxybenzaldehyde for simultaneous preconcentration and removal of gold(III), palladium(II), copper(II) and silver(I) (Journal of Industrial and Engineering Chemistry, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - protocatechuic aldehyde
- protocatechualdehyde
- rancinamycin IV
- protocatechualdehyde, formyl-14C-labeled
- protocatechualdehyde, 3H-labeled
-
SMILESC1=CC(=C(C=C1C=O)O)O
-
InChIKeyIBGBGRVKPALMCQ-UHFFFAOYSA-N
- Pubchem - 3,4-Dihydroxybenzaldehyde
- Wikipedia - protocatechualdehyde
Protocatechuic aldehyde is a phenolic aldehyde, a compound released from cork stoppers into wine. This molecule can be used as a precursor in the vanillin synthesis by biotransformation by cell cultures of Capsicum frutescens, a type of Chili pepper. It is also found in the mushroom Phellinus linteus.
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Similar Compounds
3,4,5-Trihydroxybenzaldehyde
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3-hydroxybenzaldehyde
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3,5-Dihydroxybenzaldehyde
(26153-38-8)
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3-Hydroxy-4-methoxybenzaldehyde
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2,4,5-trihydroxybenzaldehyde
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3',4'-Dihydroxyacetophenone
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Vanillin
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2,3,4-Trihydroxybenzaldehyde
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3,4-Dimethoxybenzaldehyde
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2,3-Dihydroxybenzaldehyde
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4-Hydroxy-2-methylbenzaldehyde
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3,4-Dihydroxy-5-methoxybenzaldehyde
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SYRINGALDEHYDE
(134-96-3)
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3,4-Dihydroxybenzophenone
(10425-11-3)
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3-Ethoxy-4-hydroxybenzaldehyde
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3,4-Dihydroxybenzylamine hydrobromide
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2,5-Dihydroxybenzaldehyde
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3-Methoxybenzaldehyde
(591-31-1)
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3,4-Dimethoxy-5-hydroxybenzaldehyde
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3,4-Dihydroxybenzonitrile
(17345-61-8)
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3,4,5-TRIMETHOXYBENZALDEHYDE
(86-81-7)
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4-Ethoxy-3-methoxybenzaldehyde
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2,4-DIHYDROXYBENZALDEHYDE
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99-40-1
(99-40-1)
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3-Ethoxy-4-methoxybenzaldehyde
(1131-52-8)
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Methyl 3,4-dihydroxybenzoate
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3,4-Diethoxybenzaldehyde
(2029-94-9)
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4,5-Dimethoxy-2-methylbenzaldehyde
(7721-62-2)
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2,6-Dimethyl-4-hydroxybenzaldehyde
(70547-87-4)
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3,4-Dihydroxybenzhydrazide
(39635-11-5)
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3-Bromo-4,5-dihydroxybenzaldehyde
(16414-34-9)
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3'-Hydroxyacetophenone
(121-71-1)
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3-HYDROXY-4-METHOXYBENZOIC ACID
(645-08-9)
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(110943-74-3)
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2-Methoxy-5-methylphenol
(1195-09-1)
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4-methoxy-3-(methoxymethoxy)benzaldehyde
(5779-98-6)
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2,4,6-Trihydroxybenzaldehyde
(487-70-7)
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2,4-Dihydroxy-5-methoxybenzaldehyde
(51061-83-7)
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6100-74-9
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3,5-Dimethoxybenzaldehyde
(7311-34-4)
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4-(allyloxy)-3-methoxybenzaldehyde
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Orcinol
(504-15-4)
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3-Hydroxy-2-methylbenzaldehyde
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2-Hydroxy-4-methylbenzaldehyde
(698-27-1)
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2-METHOXY-4-METHYLPHENOL
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METHYL GALLATE
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3-Hydroxybenzoic acid
(99-06-9, 10476-50-3)
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4-Methoxybenzaldehyde
(123-11-5, 50984-52-6)
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1 safety hazard
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342592-62-5
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(121-34-6)
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428847-37-4
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Dopamine hydrochloride
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29668-44-8
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4-Hydroxybenzamide
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3-propoxybenzaldehyde
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3,4-Dihydroxybenzaldehyde
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