477532
5-tert-Butyl-2-hydroxybenzaldehyde
98%
Synonym(s):
5-tert-Butylsalicylaldehyde
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About This Item
Linear Formula:
(CH3)3CC6H3(OH)CHO
CAS Number:
Molecular Weight:
178.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
InChI
1S/C11H14O2/c1-11(2,3)9-4-5-10(13)8(6-9)7-12/h4-7,13H,1-3H3
SMILES string
CC(C)(C)c1ccc(O)c(C=O)c1
InChI key
ZVCQQLGWGRTXGC-UHFFFAOYSA-N
assay
98%
refractive index
n20/D 1.539 (lit.)
bp
251-252 °C/729 mmHg (lit.)
density
1.039 g/mL at 25 °C (lit.)
functional group
aldehyde
Quality Level
General description
5-tert-Butyl-2-hydroxybenzaldehyde is a 5-substituted 2-hydroxy aromatic aldehyde. It participates in the synthesis of Schiff base appended porphyrazine.
Application
5-tert-Butyl-2-hydroxybenzaldehyde may be used in the synthesis of the following organic ligands:
- 5-tert-butyl-2-hydroxybenzaldehyde thiosemicarbazone (THTB)
- 4-tert-butyl-2-(4,5-dimethyl-1H-imidazol-2-yl)phenol
- 2-tert-butyl-6-(4,5-diphenyl-1H-imidazol-2-yl)phenol
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
219.2 °F - closed cup
flash_point_c
104 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Preparation of new class composite adsorbent for enhanced palladium (II) detection and recovery.
Awual MR, et al.
Sensors and Actuators B, Chemical, 209, 790-797 (2015)
Porphyrazines as molecular scaffolds: periphery-core spin coupling between metal ions of a schiff base porphyrazine.
Min Zhao et al.
Angewandte Chemie (International ed. in English), 42(4), 462-465 (2003-02-06)
A novel facial composite adsorbent for enhanced copper (II) detection and removal from wastewater.
Awual MR.
Chemical Engineering Journal, 266, 368-375 (2015)
Ligand characteristics and in situ generation of Pd active species towards C-C coupling using series of 2-(1H-imidazol-2-yl) phenols.
Eseola AO, et al.
J. Mol. Catal. A: Chem., 387, 112-122 (2014)
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