CAS 22775-40-2
:Ethyl 2-hydroxy-5-methoxybenzoate
Description:
Ethyl 2-hydroxy-5-methoxybenzoate, with the CAS number 22775-40-2, is an organic compound that belongs to the class of benzoates. It features a benzoic acid derivative structure, characterized by the presence of an ethyl ester group, a hydroxyl group (-OH), and a methoxy group (-OCH3) attached to the aromatic ring. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. Ethyl 2-hydroxy-5-methoxybenzoate is known for its potential applications in the fields of pharmaceuticals, cosmetics, and as a flavoring agent due to its pleasant aroma. It exhibits moderate solubility in organic solvents and limited solubility in water, which is common for many aromatic compounds. The presence of the hydroxyl group contributes to its reactivity, allowing for potential participation in various chemical reactions, such as esterification or etherification. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.
Formula:C10H12O4
InChI:InChI=1S/C10H12O4/c1-3-14-10(12)8-6-7(13-2)4-5-9(8)11/h4-6,11H,3H2,1-2H3
InChI key:InChIKey=QFDVMOCQOGCDKA-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=CC(OC)=CC=C1O
Synonyms:- 2-Hydroxy-5-methoxy-benzoic acid ethyl ester
- Benzoic acid, 2-hydroxy-5-methoxy-, ethyl ester
- Brn 2095070
- Ethyl 2-Hydroxy-5-Methoxybenzoate
- S 29
- Salicylic acid, 5-methoxy-, ethyl ester
- m-Anisic acid, 6-hydroxy-, ethyl ester
- m-Anisic acid, 6-hydroxy-, ethyl ester (8CI)
- Ethyl 5-methoxysalicylate
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Found 3 products.
Ethyl 2-hydroxy-5-methoxybenzoate
CAS:<p>Ethyl 2-hydroxy-5-methoxybenzoate (EHMB) is a phenolic compound that belongs to the group of salicylic acid. It is a natural product present in crucifers such as cabbage, broccoli, and cauliflower. EHMB has been shown to induce apoptosis in human leukemia cells through the inhibition of DNA methylation. The results showed that EHMB induces apoptosis in human leukemia cells by targeting the epigenetic regulator protein MLL1, which inhibits DNA methyltransferase 1 activity and leads to decreased levels of 5mC. EHMB also induces apoptosis in lung cancer cells by inhibiting cell proliferation and inducing cell death through the inhibition of GTPase activity, which leads to decreased levels of cyclin D1 and increased levels of p27. EHMB also regulates stem cell function by modulating gene expression; it has been shown that this compound can promote stem cell-like properties in mouse embryonic fibrobl</p>Formula:C10H12O4Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:196.2 g/mol
