InChI key
FMUYQRFTLHAARI-UHFFFAOYSA-N
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
SMILES string
CC(C)(c1ccccc1)c2ccc(O)c(c2)C(C)(C)c3ccccc3
assay
95%
form
solid
bp
206 °C/15 mmHg (lit.)
mp
63-65 °C (lit.)
General description
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.
Application
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).
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
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
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
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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