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Chemical Description |
4-hydroxybenzaldehyde is an organic compound with a hydroxyl group and an aldehyde group. |
Chemical Composition and Structure |
4-Hydroxybenzaldehyde (4-HBA) is an organic compound belonging to the class of hydroxybenzaldehydes. It is characterized by a benzene ring with a hydroxyl group (-OH) and an aldehyde group (-CHO) attached at the para position. |
Sources |
4-Hydroxybenzaldehyde is found naturally in plants such as Gastrodia elata (Tianma) and Vanilla planifolia (vanilla orchid). It can also be synthesized chemically. |
Mechanism of Action |
4-Hydroxybenzaldehyde has been studied for its various biological activities, including its ability to inhibit GABA transaminase, modulate bacterial metabolism, and act as a flavoring agent. Its mechanism of action involves interactions with specific molecular targets, such as enzymes and receptors. |
InChI:InChI=1/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H
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4-(1,3-dithiolan-2-yl)phenol
4-nitro-phenol
4-hydroxy-3-nitrobenzaldehyde
4-hydroxy-benzaldehyde
4-[1,3]dithiolan-2-yl-2-nitro-phenol
Conditions | Yield |
---|---|
With
bismuth(III) nitrate; water;
In
benzene;
at 20 ℃;
for 8h;
Product distribution;
|
methyl p-hydroxycinnamate
4-nitro-phenol
3‐nitro‐p‐coumaric acid methyl ester
C10H11ClO4
4-hydroxy-benzaldehyde
Conditions | Yield |
---|---|
With
hydrogenchloride; water; dihydrogen peroxide; sodium hydroxide; sodium nitrite;
In
aq. buffer;
|
formaldehyd
sodium phenoxide
formic acid
4-acetoxybenzoyl chloride
(E)-3-(4-hydroxyphenyl)-N-phenylacrylamide
4-hydroxy-3-(piperidin-1-ylmethyl)benzaldehyde
2-(4-hydroxyphenyl)-2-(piperidin-1-yl)acetonitrile
2,5-dimorpholinocyclohexa-2,5-diene-1,4-dione
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