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Merck

372129

Sigma-Aldrich

2,4-Bis-(α,α-dimethylbenzyl)-phenol

95%

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About This Item

Lineare Formel:
[C6H5C(CH3)2]2C6H3OH
CAS-Nummer:
Molekulargewicht:
330.46
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

95%

Form

solid

bp

206 °C/15 mmHg (lit.)

mp (Schmelzpunkt)

63-65 °C (lit.)

SMILES String

CC(C)(c1ccccc1)c2ccc(O)c(c2)C(C)(C)c3ccccc3

InChI

1S/C24H26O/c1-23(2,18-11-7-5-8-12-18)20-15-16-22(25)21(17-20)24(3,4)19-13-9-6-10-14-19/h5-17,25H,1-4H3

InChIKey

FMUYQRFTLHAARI-UHFFFAOYSA-N

Allgemeine Beschreibung

2,4-Bis(α,α-dimethylbenzyl)phenol is reported to possess antihistaminic activity. Structure of 2,4-bis(α,α-dimethylbenzyl)phenol is reported to have a torsion angle of 129.95(13)° for the C-C bond that connects the benzyl carbon to the phenol ring ortho to the OH group.

Anwendung

2,4-Bis(α,α-dimethylbenzyl)phenol may be used in the preparation of a novel ligand, 2,2′-methylenebis(4,6-di(1-methyl-1-phenylethyl)phenol) (MMPEP-H2).

Piktogramme

Exclamation markEnvironment

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Bryan
Acta crystallographica. Section C, Crystal structure communications, 56 (Pt 8), 1046-1047 (2000-08-16)
The structure of the title compound, 2, 4-bis(1-methyl-1-phenylethyl)phenol, C(24)H(26)O, was found to have a torsion angle of 129.95 (13) degrees for the C-C bond that connects the benzyl carbon to the phenol ring ortho to the OH group. A value
Zhuo Wang et al.
Journal of chromatography. A, 1616, 460793-460793 (2019-12-24)
With 4,4'-diaminoterphenyl and phloroglucinol as the monomers, Azo-linked porous organic polymer (PP) was prepared by a green mild azo reaction. Azo-PP is rich in phenolic hydroxyl groups and benzene rings, which can form intermolecular hydrogen bonds with the phenolic hydroxyl
A highly efficient catalyst for the ?living? and ?immortal? polymerization of e-caprolactone and L-lactide.
Liu Y-C, et al.
Macromolecules, 34(18), 6196-6201 (2001)
María J Duart et al.
Journal of medicinal chemistry, 49(12), 3667-3673 (2006-06-09)
Molecular topology was used to achieve a mathematical model capable of classifying compounds according to their antihistaminic activity and low sedative effects. By application of this model of activity to databases containing chemical reagents and drugs exhibiting other pharmacological activity
Alan J Bergmann et al.
Analytical and bioanalytical chemistry, 412(19), 4527-4536 (2020-05-28)
Food contact materials (FCM) may contain complex mixtures of estrogenic chemicals. A yeast estrogen screen performed on high performance thin-layer chromatography plates (planar-YES, P-YES) is promising for analysis of such mixtures, as it could allow for better elucidation of effects

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