554154
4-tert-Butyl-2,6-diformylphenol
96%
Synonym(s):
5-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedicarboxaldehyde
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About This Item
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Quality Level
Assay
96%
mp
99-103 °C (lit.)
functional group
aldehyde
SMILES string
CC(C)(C)c1cc(C=O)c(O)c(C=O)c1
InChI
1S/C12H14O3/c1-12(2,3)10-4-8(6-13)11(15)9(5-10)7-14/h4-7,15H,1-3H3
InChI key
WQNTWZJPCLUXQC-UHFFFAOYSA-N
Related Categories
General description
4-tert-Butyl-2,6-diformylphenol can be prepared from 4-tert-butylphenol and hexamethylenetetramine.
Application
4-tert-Butyl-2,6-diformylphenol may be used to synthesize:
- symmetrical macrocyclic Schiff′s base
- 2,6-bis(N-(4′-methyl-2′-hydroxyphenyl)iminomethyl)-4-tert-butylphenol
- isostructural C3-symmetrical triple stranded dinuclear lanthanide analogs
- 5-tert-butyl-2 hydroxy-isophthalaldehyde-bis-2-pyridinehydrazone via reaction with 2-hydrazinopyridine
- 5-tert-butyl-2-hydroxyisophthalaldehyde-bisphenylhydrazone via reaction with phenylhydrazine
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Binuclear and polynuclear transition metal complexes with macrocyclic ligands. 2. New macrocyclic Schiff" s base in the reaction of 4-tert-butyl-2, 6-diformylphenol with 1, 2-diaminobenzene. Synthesis and structural, spectroscopic, and theoretical study.
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A series of isostructural C3-symmetrical triple stranded dinuclear lanthanide [Ln2L3](NO3)3 molecules have been synthesized using subcomponent self-assembly of Ln(NO3)3 with 2-(methylhydrazino)benzimidazole and 4-tert-butyl-2,6-diformylphenol, where Ln = Tb (1), Dy (2), Ho (3), Er (4), Tm (5), and Yb (6). The
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