CAS 500-99-2
:3,5-Dimethoxyphenol
Description:
3,5-Dimethoxyphenol, with the CAS number 500-99-2, is an organic compound characterized by a phenolic structure with two methoxy groups (-OCH3) attached to the aromatic ring at the 3 and 5 positions. This compound typically appears as a white to off-white crystalline solid and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water due to its hydrophobic nature. It exhibits properties typical of phenolic compounds, including antioxidant activity and potential applications in various fields such as pharmaceuticals, cosmetics, and as a chemical intermediate. The presence of methoxy groups enhances its electron-donating ability, influencing its reactivity and stability. 3,5-Dimethoxyphenol can undergo typical electrophilic aromatic substitution reactions, making it a versatile building block in organic synthesis. Additionally, it may exhibit biological activities, including antimicrobial and anti-inflammatory effects, which are of interest in medicinal chemistry. Proper handling and safety precautions should be observed, as with all chemical substances, to mitigate any potential hazards.
Formula:C8H10O3
InChI:InChI=1S/C8H10O3/c1-10-7-3-6(9)4-8(5-7)11-2/h3-5,9H,1-2H3
InChI key:InChIKey=XQDNFAMOIPNVES-UHFFFAOYSA-N
SMILES:O(C)C1=CC(OC)=CC(O)=C1
Synonyms:- 1-Hydroxy-3,5-dimethoxybenzene
- 3,5-Dimethoxy Phenol
- NSC 70955
- Phenol, 3,5-dimethoxy-
- Phloroglucinol dimethyl ether
- Taxicatigenin
- 3,5-Dimethoxyphenol
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Found 11 products.
3,5-Dimethoxyphenol, 98%
CAS:<p>3,5-dimethoxyphenol is a marker for poisoning from Taxus baccata. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU referen</p>Formula:C8H10O3Purity:98%Color and Shape:White to pale brown or yellow, Crystals or powder or crystalline powder or fused solidMolecular weight:154.163,5-Dimethoxyphenol
CAS:3,5-DimethoxyphenolFormula:C8H10O3Purity:≥95%Color and Shape: yellow crystalline solidMolecular weight:154.16g/mol3,5-Dimethoxyphenol
CAS:Formula:C8H10O3Purity:≥ 98.0%Color and Shape:White to orange powder or solid crystalsMolecular weight:154.163,5-Dimethoxyphenol
CAS:3,5-Dimethoxyphenol (Phloroglucinol dimethyl ether) as a marker of Taxus poisoning, being present in all species of Taxus.Formula:C8H10O3Purity:98%Color and Shape:Slightly Pink To Yellow Crystalline PowderMolecular weight:154.163,5-Dimethoxyphenol
CAS:<p>Applications 3,5-Dimethoxyphenol is a phenol derivative as antinitrosating agent.<br>References Marletta, M., et al.: Chem. Res. Toxicol., 1, 249 (1988), Caulfield, J., et al.: J. Biol. Chem., 273, 12689 (1998), Wang, P., et al.: Chem. Rev., 102, 1091 (2002),<br></p>Formula:C8H10O3Color and Shape:Off White SolidMolecular weight:154.163,5-Dimethoxyphenol
CAS:<p>3,5-Dimethoxyphenol (3,5-DMP) is a synthetic chemical compound that is used for the preparation of sulfonamides. It is prepared by the reaction of 3,5-dimethoxybenzene and trifluoromethanesulfonic acid in aqueous solution. The reaction yield can be increased by adding trimethylsilyl chloride to the solvent system. 3,5-DMP reacts with sulfite to form 3,5-dihydroxyphenylsulfate. The enzyme preparations are extracted from plant cells and then purified by chromatography on silica gel. This chemical reacts with divalent metal ions such as magnesium and calcium in an acidic environment to form salts. These salts react with hydrogen sulfate in an acidic environment to produce 3,5-dihydroxyphenylsulfate. This product also undergoes a kinetic method where it reacts with oxygen to form hydrogen per</p>Formula:C8H10O3Purity:Min. 95%Color and Shape:PowderMolecular weight:154.16 g/mol3,5-Dimethoxyphenol
CAS:Formula:C8H10O3Purity:96%Color and Shape:Solid, Low Melting SolidMolecular weight:154.1653,5-Dimethoxyphenol
CAS:Formula:C8H10O3Purity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:154.17









