Weight | 234.339 g/mol |
---|---|
Formula | C15H22O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3,5-Di-tert-butyl-2-hydroxybenzaldehyde (37942-07-7)
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- Thermodynamic study on hydroxybenzaldehyde derivatives: 3- and 4-Hydroxybenzaldehyde isomers and 3,5-di-tert-butyl-2-hydroxybenzaldehyde (The Journal of Chemical Thermodynamics, 2010)
- Synthesis of substituted 3,4-dihydropyrimidin-2(1H)-ones and pyrimidin-2(1H)-ones by the Biginelli reaction with 3,5-Di-tert-butyl-4-hydroxybenzaldehyde (Russian Journal of Organic Chemistry, 2009)
- Photo- and thermochromic mannich bases. 1. Mannich bases from 3,5-di-tert-butyl-4-hydroxybenzaldehyde and 2-naphthols (Russian Chemical Bulletin, 1992)
- 3,5-Di-tert-butyl-2-hydroxybenzaldehyde (Acta Crystallographica Section E-structure Reports Online, 2004)
- ChemInform Abstract: Synthesis of Substituted 3,4-Dihydropyrimidin-2(1H)-ones and Pyrimidin-2(1H)-ones by the Biginelli Reaction with 3,5-Di-tert-butyl-4-hydroxybenzaldehyde. (ChemInform, 2010)
- ChemInform Abstract: Photo- and Thermochromic Mannich Bases. Part 1. Mannich Bases (IV) from 3,5-Di-tert-butyl-4-hydroxybenzaldehyde and 2-Naphthols. (ChemInform, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)C1=CC(=C(C(=C1)C=O)O)C(C)(C)C
-
InChIKeyRRIQVLZDOZPJTH-UHFFFAOYSA-N
- Pubchem - 3,5-Di-tert-butyl-2-hydroxybenzaldehyde
- Wikipedia - 3,5-Di-tert-butylsalicylaldehyde
3,5'-Di-tert-butylsalicylaldehyde is an organic compound. It is a pale yellow solid. This aldehyde is a building block for preparing salen ligands.
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Synthesis
2,4-DI-TERT-BUTYL-6-(HYDROXYMETHYL)PHENOL
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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