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Merck

140406

Sigma-Aldrich

3,5-Ditert-butyl-4-hydroxybenzaldehyde

99%

Sinónimos:

2,6-Di-tert-Butyl-4-formylphenol, 3,5-Di-tert-butyl-4-hydroxybenzaldehyde

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About This Item

Fórmula empírica (notación de Hill):
C15H22O2
Número de CAS:
Peso molecular:
234.33
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

99%

form

solid

solubility

ethanol: soluble 50 mg/mL, clear to slightly hazy (yellow to orange to light red-brown)

SMILES string

CC(C)(C)c1cc(C=O)cc(c1O)C(C)(C)C

InChI

1S/C15H22O2/c1-14(2,3)11-7-10(9-16)8-12(13(11)17)15(4,5)6/h7-9,17H,1-6H3

InChI key

DOZRDZLFLOODMB-UHFFFAOYSA-N

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Application

3,5-Di-tert-butyl-4-hydroxybenzaldehyde can be used as a starting material to synthesize:

  • Biodegradable polyazomethine hydrogels by reacting with melamine via oxidative polymerization reaction.
  • 4-(1H-benzimidazol-2-yl)-2,6-di-tert butyl-phenol by treating with 1,2-phenylenediamine in ethanol.
  • 2-{(3,5-di-tert-butyl-4-hydroxyphenyl)methylene}-4-cyclopentene-1,3-dione (TX-1123) as a potent protein tyrosine kinase inhibitor.
  • Polyazomethine and ascorbic acid-based selective and sensitive fluorescent chemosensor for the detection of Al and Fe metal ions.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificados de análisis (COA)

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Melamine-based poly (azomethine) hydrogels: Mechanical, biodegradability, drug loading and antibacterial properties
Kamaci M and Kaya I
European Polymer Journal, 108, 107-115 (2018)
Highly stabilized phenoxyl radicals with hydrogen-bonding capability.
Xie C and Lahti PM.
Tetrahedron Letters, 40(23), 4305-4308 (1999)
A dual responsive colorimetric sensor based on polyazomethine and ascorbic acid for the detection of Al (III) and Fe (II) ions
Kamaci UD, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 254, 119650-119650 (2021)
Highly stabilized phenoxyl radicals with hydrogen-bonding capability
Xie Chunping and Lahti PM
Tetrahedron Letters, 40(23), 4305-4308 (1999)
Hitoshi Hori et al.
Bioorganic & medicinal chemistry, 10(10), 3257-3265 (2002-08-02)
A series of 2-hydroxyarylidene-4-cyclopentene-1,3-diones were designed, synthesized, and evaluated with respect to protein tyrosine kinase (PTK) inhibition, mitochondrial toxicity, and antitumor activity. Our results show that the cyclopentenedione-derived TX-1123 is a more potent antitumor tyrphostin and also shows lower mitochondrial

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