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Merck
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文件

140406

Sigma-Aldrich

3,5-Ditert-butyl-4-hydroxybenzaldehyde

99%

别名:

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

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About This Item

经验公式（希尔记法）:
C15H22O2
CAS号:
1620-98-0
分子量:
234.33
EC號碼:
216-592-0
MDL號碼:
MFCD00008826
分類程式碼代碼:
12352100
PubChem物質ID:
24848468
NACRES:
NA.22

化驗

99%

形狀

solid

溶解度

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

SMILES 字串

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 密鑰

DOZRDZLFLOODMB-UHFFFAOYSA-N

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應用

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.

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves

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Highly stabilized phenoxyl radicals with hydrogen-bonding capability.
Xie C and Lahti PM.
Tetrahedron Letters, 40(23), 4305-4308 (1999)
Melamine-based poly (azomethine) hydrogels: Mechanical, biodegradability, drug loading and antibacterial properties
Kamaci M and Kaya I
European Polymer Journal, 108, 107-115 (2018)
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)
TX-1123: an antitumor 2-hydroxyarylidene-4-cyclopentene-1, 3-dione as a protein tyrosine kinase inhibitor having low mitochondrial toxicity
Hori H, et al.
Bioorganic & Medicinal Chemistry Letters, 10(10), 3257-3265 (2002)
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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