95-01-2
Chemical Structure
2,4-Dihydroxybenzaldehyde
- CAS No.: 95-01-2
- Formula:C7H6O3
- Molecular Weight:138.12
IUPAC Name: 2,4-dihydroxybenzaldehyde
InChIKey: IUNJCFABHJZSKB-UHFFFAOYSA-N
SMILES: O=CC1=CC=C(O)C=C1O
Biological Activity: 2,4-Dihydroxybenzaldehyde is an endogenous metabolite. 2,4-Dihydroxybenzaldehyde is a pharmaceutical intermediate that can be used to synthesize various Schiff base compounds. 2,4-Dihydroxybenzaldehyde exhibits significant anti angiogenic, anti-inflammatory, and analgesic activities. 2,4-Dihydroxybenzaldehyde reduces the production of NO and ROS by inhibiting the expression of iNOS and COX-2. 2,4-Dihydroxybenzaldehyde is commonly used in the study of inflammatory conditions[1][2].
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2,4-Dihydroxybenzaldehyde | 99.90% | 2,4-Dihydroxybenzaldehyde is an endogenous metabolite. 2,4-Dihydroxybenzaldehyde is a pharmaceutical intermediate that can be used to synthesize various Schiff base compounds. 2,4-Dihydroxybenzaldehyde exhibits significant anti angiogenic, anti-inflammatory, and analgesic activities. 2,4-Dihydroxybenzaldehyde reduces the production of NO and ROS by inhibiting the expression of iNOS and COX-2. 2,4-Dihydroxybenzaldehyde is commonly used in the study of inflammatory conditions. | ||||||||||||||||||||
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2,4-Dihydroxybenzaldehyde (Standard) | ≥98% | 2,4-Dihydroxybenzaldehyde (Standard) is the analytical standard of 2,4-Dihydroxybenzaldehyde. This product is intended for research and analytical applications. 2,4-Dihydroxybenzaldehyde is an endogenous metabolite. 2,4-Dihydroxybenzaldehyde is a pharmaceutical intermediate that can be used to synthesize various Schiff base compounds. 2,4-Dihydroxybenzaldehyde exhibits significant anti angiogenic, anti-inflammatory, and analgesic activities. 2,4-Dihydroxybenzaldehyde reduces the production of NO and ROS by inhibiting the expression of iNOS and COX-2. 2,4-Dihydroxybenzaldehyde is commonly used in the study of inflammatory conditions. | ||||||||||||||||||||
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- [1]. Murtaza S, et al. Synthesis, biological activities and docking studies of novel 2, 4-dihydroxybenzaldehyde based Schiff base. Medicinal Chemistry Research, 2016, 25(12): 2860-2871.
- [2]. Jung H J, et al. Evaluation on pharmacological activities of 2, 4-dihydroxybenzaldehyde. Biomolecules & Therapeutics, 2009, 17(3): 263-269.
