CAS 830-79-5
:2,4,6-Trimethoxybenzaldehyde
Description:
2,4,6-Trimethoxybenzaldehyde, with the CAS number 830-79-5, is an aromatic aldehyde characterized by the presence of three methoxy (-OCH₃) groups attached to a benzaldehyde structure. This compound features a benzene ring substituted at the 2, 4, and 6 positions with methoxy groups, which significantly influence its chemical properties and reactivity. It is typically a colorless to pale yellow liquid with a sweet, floral aroma, making it of interest in the fragrance and flavor industries. The presence of the aldehyde functional group (-CHO) contributes to its reactivity, allowing it to participate in various chemical reactions, including condensation and oxidation. 2,4,6-Trimethoxybenzaldehyde is also soluble in organic solvents, such as ethanol and ether, but has limited solubility in water due to its hydrophobic methoxy groups. Its unique structure and properties make it a valuable compound in organic synthesis and research applications, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C10H12O4
InChI:InChI=1S/C10H12O4/c1-12-7-4-9(13-2)8(6-11)10(5-7)14-3/h4-6H,1-3H3
InChI key:InChIKey=CRBZVDLXAIFERF-UHFFFAOYSA-N
SMILES:C(=O)C1=C(OC)C=C(OC)C=C1OC
Synonyms:- Benzaldehyde, 2,4,6-trimethoxy-
- 2,4,6-Trimethoxybenzaldehyde
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Found 8 products.
2,4,6-Trimethoxybenzaldehyde
CAS:Formula:C10H12O4Purity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:196.202,4,6-Trimethoxybenzaldehyde, 98%
CAS:<p>2,4,6-Trimethoxybenzaldehyde was used in the preparation and characterization of three RNA-specific fluorescent probes and their use in live cell imaging. It was used as starting reagent for the regioselective synthesis of new ()-8-alkyl-5,7-dihydroxy-4-(4-hydroxyphenyl)-3,4-dihydrocoumarins. This T</p>Formula:C10H12O4Purity:98%Color and Shape:White to cream, Powder or crystalline powderMolecular weight:196.202,4,6-Trimethoxybenzaldehyde
CAS:Formula:C10H12O4Purity:98%Color and Shape:SolidMolecular weight:196.19992,4,6-Trimethoxybenzaldehyde
CAS:Formula:C10H12O4Purity:≥ 98.0%Color and Shape:White to off-white or light yellow crystalline powderMolecular weight:196.202,4,6-Trimethoxybenzaldehyde
CAS:Formula:C10H12O4Purity:95%Color and Shape:Solid, Chunks or Crystalline PowderMolecular weight:196.2022,4,6-Trimethoxybenzaldehyde
CAS:<p>2,4,6-Trimethoxybenzaldehyde</p>Formula:C10H12O4Purity:98%Color and Shape: beige solidMolecular weight:196.20g/mol2,4,6-Trimethoxybenzaldehyde
CAS:<p>2,4,6-Trimethoxybenzaldehyde is a chemical compound that is used as an intermediate in organic chemistry. It has been shown to have antiviral effects on influenza A virus by inhibiting the enzyme neuraminidase. This inhibition prevents the release of viruses from infected cells and thus prevents viral replication. 2,4,6-Trimethoxybenzaldehyde also inhibits the growth of cancer cells in vitro and has minimal toxicity to normal cells. This chemical has been shown to inhibit the reaction mechanism of proton pumps in mammalian cells, which may be due to its ability to inhibit p2y receptors or nitrogen atoms. 2,4,6-Trimethoxybenzaldehyde can also be used as a solvent for pharmaceutical preparations and as a reagent in x-ray diffraction data analysis.</p>Formula:C10H12O4Purity:Min. 95%Color and Shape:PowderMolecular weight:196.2 g/mol2,4,6-Trimethoxybenzaldehyde
CAS:Controlled Product<p>Applications 2,4,6-Trimethoxybenzaldehyde is a reagent used in the synthesis of anticancer/antiproliferative chalcones, chromenones and flavonols. Antip<br>References Dias, T. et al.: Eur. J. Med. Chem., 65, 500 (2013); Chand, K. et al.: Can. J. Chem., 91, 741 (2013);<br></p>Formula:C10H12O4Color and Shape:NeatMolecular weight:196.2







