CAS 3541-42-2
:2-Hydroxycinnamaldehyde
Description:
2-Hydroxycinnamaldehyde, also known as o-hydroxycinnamaldehyde, is an organic compound characterized by its aromatic structure, which includes a hydroxyl group (-OH) and an aldehyde group (-CHO) attached to a cinnamic acid backbone. This compound typically appears as a yellow to brown crystalline solid with a characteristic sweet, floral odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water. 2-Hydroxycinnamaldehyde exhibits various biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties, making it of interest in pharmaceuticals and food preservation. Its chemical reactivity is influenced by the presence of the hydroxyl and aldehyde functional groups, allowing it to participate in various chemical reactions, such as condensation and oxidation. Additionally, it is often used as a flavoring agent and in the synthesis of other organic compounds. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes.
Formula:C9H8O2
InChI:InChI=1S/C9H8O2/c10-7-3-5-8-4-1-2-6-9(8)11/h1-7,11H
InChI key:InChIKey=BSDNZCQPDVTDET-UHFFFAOYSA-N
SMILES:C(=CC=O)C1=C(O)C=CC=C1
Synonyms:- (2E)-3-(2-hydroxyphenyl)prop-2-enal
- 2-Hydroxycinnamaldehyde
- 2-Hydroxycinnamic aldehyde
- 2-Propenal, 3-(2-hydroxyphenyl)-
- 3-(2-Hydroxyphenyl)-2-propenal
- 3-(2-Hydroxyphenyl)Prop-2-Enal
- 3-(2-Hydroxyphenyl)acrylaldehyde
- Cinnamaldehyde, o-hydroxy-
- NSC 114588
- o-Hydroxycinnamaldehyde
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Found 4 products.
2-Hydroxycinnamaldehyde
CAS:Formula:C9H8O2Purity:>98.0%(HPLC)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:148.163-(2-Hydroxyphenyl)Acrylaldehyde
CAS:<p>3-(2-Hydroxyphenyl)Acrylaldehyde</p>Purity:98%Molecular weight:148.16g/mol2-Hydroxycinnamaldehyde
CAS:<p>2-Hydroxycinnamaldehyde is a chemical compound that has been shown to inhibit cancer cell growth and induce apoptosis in vitro. 2-Hydoxycinnamaldehyde is a member of the class of phenylpropanoids, which has been shown to bind to DNA and inhibit the expression of β-catenin. It also has anti-angiogenic effects by inhibiting vascular endothelial growth factor (VEGF) production and VEGF receptor activation. The study of 2-hydroxycinnamaldehyde was carried out using both an in vivo model and a cell culture model. The in vivo model used was the mouse skin cancer model, while the cell culture models were human colon cancer cells (SW620) and human lung cancer cells (HCT116). Swelling, necrosis, cytotoxicity, and apoptosis were observed in both types of models after treatment with 2-hydroxycinnamaldehyde. The hydroxyl group on the catech</p>Formula:C9H8O2Purity:Min. 95%Color and Shape:PowderMolecular weight:148.16 g/mol



