Interesting facts
Interesting Facts about 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol
4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol, also known as a branched chain phenolic compound, exhibits a unique structure that combines both ethyl and hydroxyphenyl groups. This intriguing arrangement contributes to its diverse applications and properties. Here are some interesting points:
- Versatile Ingredient: This compound often functions as a key ingredient in various chemical formulations, including cosmetic products, pharmaceuticals, and industrial applications.
- Antioxidant Properties: The presence of hydroxyl groups in its structure allows this compound to exhibit significant antioxidant activity, which helps combat oxidative stress in biological systems.
- Potential Health Benefits: Some studies suggest that derivatives of phenolic compounds can have protective effects against diseases such as cancer and heart disease, making them a focus of ongoing research.
- Functionalization: The ability to modify the phenolic structure enables chemists to tailor specific properties for targeted applications, enhancing its functionality and efficiency in usage.
- Environmental Impact: As with many organic compounds, understanding the environmental fate of this compound is essential, especially regarding its degradation and potential accumulation in ecosystems.
In conclusion, 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol serves as a prime example of how organic compounds can play vital roles across various fields. Its rich chemistry and promising utility make it a subject of interest for further exploration and understanding.
Synonyms
hexestrol
5635-50-7
Dihydrodiethylstilbestrol
Vitestrol
Hexoestrolum
4,4'-(1,2-Diethylethylene)diphenol
Exestrol
Stilbestrol, dihydro-
4,4'-(hexane-3,4-diyl)diphenol
Phenol, 4,4'-(1,2-diethyl-1,2-ethanediyl)bis-
4-[4-(4-hydroxyphenyl)hexan-3-yl]phenol
Hexane, 3,4-bis(4-hydroxyphenyl)-
Synoestrolum
Phenol, 4,4'-(1,2-diethylethylene)di-
CHEBI:31669
3,4-Bis(p-hydroxyphenyl)hexane
Hexanestrol
NSC 9894
Hormoestrol; Mesohexestrol; NSC 9894; Sinestrol
Esestrolo [DCIT]
Hexestrolum
Esestrolo
Hexestrolum [INN-Latin]
MFCD00068996
Hexestrol [INN:NF]
4,2-Diethylethylene)diphenol
SR-05000001870
EINECS 227-082-2
NSC-9894
Phenol,4'-(1,2-diethylethylene)di-
Prestwick_80
1,4-Dicyano-2,3,5,6-tetrachlorobenzene; 2,3,5,6-Tetrachloro-1,4-benzenedicarbonitrile; 2,3,5,6-Tetrachloro-1,4-dicyanobenzene; 2,3,5,6-Tetrachloroterephthalonitrile; Tetrachloroterephthalodinitrile
Spectrum_000487
Hexestrol (JAN/INN)
Prestwick0_000699
Prestwick1_000699
Prestwick2_000699
Prestwick3_000699
Spectrum2_000891
Spectrum3_000560
Spectrum4_000392
Spectrum5_001475
4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol
CHEMBL6615
Oprea1_380638
BSPBio_000857
BSPBio_002239
KBioGR_000943
KBioSS_000967
MLS002153963
DivK1c_000443
SCHEMBL154886
SPECTRUM1500632
SPBio_000702
SPBio_002778
BPBio1_000943
GTPL2823
4,4'-hexane-3,4-diyldiphenol
Hexane,4-bis(4-hydroxyphenyl)-
HMS501G05
KBio1_000443
KBio2_000967
KBio2_003535
KBio2_006103
KBio3_001739
DTXSID30859129
NINDS_000443
3,4-bis(4-hydroxyphenyl) hexane
4,4'-(3,4-Hexanediyl)diphenol
HMS1570K19
HMS1921M07
HMS2097K19
HMS2235O21
HMS3369N07
HMS3656I04
HMS3714K19
Pharmakon1600-01500632
BCP03061
QYB47612
CCG-39630
NSC229419
NSC757393
STK366320
AKOS005442984
NSC-229419
NSC-757393
4,4\'-(1,2-Diethylethylene)Diphenol
IDI1_000443
NCGC00094818-01
NCGC00094818-02
NCGC00094818-03
NCGC00094818-04
NCGC00094818-05
NCGC00094818-06
NCGC00094818-08
AC-12485
AS-56141
SMR001233302
SBI-0051565.P002
AB00052132
D0494
NS00003872
D01641
Phenol,4'-(1,2-diethyl-1,2-ethanediyl)bis-
AB00052132_08
Q5896882
SR-05000001870-1
SR-05000001870-3
SR-05000001870-4
BRD-A01078468-001-05-6
BRD-A01078468-001-08-0
BRD-A01078468-001-14-8
Solubility of 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol (C18H20O2)
The solubility of 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol is an intriguing aspect due to its complex organic structure. This compound, with its notable functional groups, exhibits certain characteristics that determine its solubility behavior:
In conclusion, while 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol demonstrates limited solubility in water due to its hydrophobic qualities, it reveals a more favorable interaction with organic solvents, highlighting the importance of molecular structure in solubility behavior.