Weight | 150.177 g/mol |
---|---|
Formula | C9H10O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3,5-Dimethyl-4-hydroxybenzaldehyde (2233-18-3)
4-hydroxy-3,5-dimethylbenzaldehyde · DMHB-3,5
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- Spectroscopic studies and biological evaluation of some transition metal complexes of azo Schiff-base ligand derived from (1-phenyl-2,3-dimethyl-4-aminopyrazol-5-one) and 5-((4-chlorophenyl)diazenyl)-2-hydroxybenzaldehyde (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- A novel oxygenation of 2,4,6-trimethylphenol to 3,5-dimethyl-4-hydroxybenzaldehyde by dioxygen with copper(II)-amine complex catalyst (Tetrahedron Letters, 1990)
- A facile synthesis of 3,5-dimethyl-4-hydroxybenzaldehyde via copper-mediated selective oxidation of 2,4,6-trimethylphenol (Catalysis Today, 2008)
- Long range 4J- and 6J-interactions in 2,6-dimethyl-3,4-dibromophenol and 3,5-dimethyl-4-hydroxybenzaldehyde (Tetrahedron Letters, 1968)
- Production of 3,5-dimethyl-4-hydroxybenzaldehyde (1989)
- ChemInform Abstract: A Novel Oxygenation of 2,4,6-Trimethylphenol to 3,5-Dimethyl-4- hydroxybenzaldehyde by Dioxygen with the Copper(II)-Amine Complex Catalyst. (ChemInform, 2010)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-hydroxy-3,5-dimethylbenzaldehyde
- DMHB-3,5
-
SMILESCC1=CC(=CC(=C1O)C)C=O
-
InChIKeyUYGBSRJODQHNLQ-UHFFFAOYSA-N
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