CAS 6248-20-0
:2,4-Dihydroxy-3-methylbenzaldehyde
Description:
2,4-Dihydroxy-3-methylbenzaldehyde, also known as 3-methyl-2,4-dihydroxybenzaldehyde, is an organic compound characterized by its aromatic structure featuring a benzaldehyde functional group along with two hydroxyl (-OH) groups and a methyl (-CH3) group. This compound typically appears as a solid at room temperature and is soluble in organic solvents due to its aromatic nature. The presence of hydroxyl groups contributes to its potential as a phenolic compound, which can exhibit antioxidant properties. Its molecular structure allows for various chemical reactivity, including potential participation in electrophilic aromatic substitution reactions. Additionally, the compound may be used in organic synthesis and as an intermediate in the production of dyes, pharmaceuticals, or other chemical products. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose risks if ingested or inhaled. Overall, 2,4-Dihydroxy-3-methylbenzaldehyde is a versatile compound with applications in various fields of chemistry.
Formula:C8H8O3
InChI:InChI=1S/C8H8O3/c1-5-7(10)3-2-6(4-9)8(5)11/h2-4,10-11H,1H3
InChI key:InChIKey=AOPMHYFEQDBXPZ-UHFFFAOYSA-N
SMILES:C(=O)C1=C(O)C(C)=C(O)C=C1
Synonyms:- 2,4-Dihydroxy-3-Methyl-Benzaldehyde
- 2,4-Dihydroxy-m-tolualdehyde
- 3-Methyl-2,4-dihydroxybenzaldehyde
- 4-Formyl-2-methylresorcinol
- Benzaldehyde, 2,4-dihydroxy-3-methyl-
- β-Resorcylaldehyde, 3-methyl-
- 2,4-Dihydroxy-3-methylbenzaldehyde
- 2,4-Dihydroxy-3-methylbenzaldehyde
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Found 5 products.
2,4-Dihydroxy-3-methylbenzaldehyde
CAS:Formula:C8H8O3Purity:98%Color and Shape:SolidMolecular weight:152.14732,4-Dihydroxy-3-methylbenzaldehyde
CAS:2,4-Dihydroxy-3-methylbenzaldehydePurity:97%Color and Shape:PowderMolecular weight:152.15g/mol2,4-Dihydroxy-3-methylbenzaldehyde
CAS:Formula:C8H8O3Purity:95%Color and Shape:Solid, Brown powderMolecular weight:152.1494-Formyl-2-methylresorcinol
CAS:Controlled Product<p>Applications 4-Formyl-2-methylresorcinol is a reactant in the synthesis of 3-benzo[b]thiophenecoumarin, with potent anti-proliferative activity against breast cancer cell lines<br>References Zhao, H., et. al.: ACS Med. Chem., Lett., 3, 327 (2012)<br></p>Formula:C8H8O3Color and Shape:NeatMolecular weight:152.15




