Interesting facts
Interesting Facts About 4-[(4-acetoxyphenyl)-cyclohexylidene-methyl]phenyl acetate
This compound, characterized by its complex structure and functional groups, presents intriguing avenues for exploration in the field of organic chemistry. Here are some engaging insights:
- Chemical Structure: The presence of multiple aromatic rings connected by a cyclohexylidene group contributes to unique properties, including potential interactions in biochemical pathways.
- Functional Applications: Compounds with similar structures may exhibit interesting pharmacological properties, making them candidates for research in medicinal chemistry.
- Synthetic Routes: The synthesis of this compound involves advanced techniques, likely requiring the use of protective groups and catalysts. Understanding these methods is crucial for any chemist.
- Potential Uses: Due to its acetoxy group, it may participate in reactions such as esterification and hydrolysis, indicating versatility in chemical reactivity.
- Research Potential: Investigations into its biochemical effects could reveal novel insights into drug design, particularly in segments like oncology or pain management.
- Interdisciplinary Links: This compound bridges areas of chemistry, pharmacology, and materials science, illustrating the interconnectedness of scientific disciplines.
In summary, 4-[(4-acetoxyphenyl)-cyclohexylidene-methyl]phenyl acetate represents a rich area for study, blending rich structural complexity with promising application potential in various scientific fields.
Synonyms
cyclofenil
2624-43-3
Ondonid
Sexovid
Cyclofenyl
Cyclopenil
Cyclophenyl
Fertodur
Ondogyne
Rehibin
Cyclophenil
Sexadieno
Oginex
Sexovar
Sanocrisin
Neoclym
ICI 48213
Ciclofenilo
F 6066
Cyclofenilum
4,4'-(Cyclohexylidenemethylene)diphenol diacetate ester
(Cyclohexylidenemethylene)-bis(4,1-phenylene) diacetate
Cyclofenilum [INN-Latin]
Ciclofenilo [INN-Spanish]
NSC 86464
H 3452
Cyclofenil [INN:BAN:DCF:JAN]
EINECS 220-089-1
ICI-48213
NSC-86464
Sexovid (TN)
F-6066
BRN 2014687
Bis(p-hydroxyphenyl)cyclohexyldienemethane diacetate
DTXSID4022866
AI3-52271
J468V64WZ1
CYCLOFENIL [MI]
CYCLOFENIL [INN]
CYCLOFENIL [JAN]
CYCLOFENIL [MART.]
Phenol, 4-((4-(acetyloxy)phenyl)cyclohexylidenemethyl)-, acetate
CYCLOFENIL [WHO-DD]
Bis-(p-hydroxyphenyl)-cyclohexylidenemethane diacetate
DTXCID002866
F6066
4,4'-(Cyclohexylidenmethylen)diphenyl diacetat
CFN
(Cyclohexylidenemethylene)bis(4,1-phenylene) diacetate
NCGC00165767-02
[4-[(4-acetyloxyphenyl)-cyclohexylidenemethyl]phenyl] acetate
p-CRESOL, alpha-CYCLOHEXYLIDENE-alpha-(p-HYDROXYPHENYL)-, DIACETATE
Cyclofenilum (INN-Latin)
Ciclofenilo (INN-Spanish)
CYCLOFENIL (MART.)
4-{[4-(acetyloxy)phenyl](cyclohexylidene)methyl}phenyl acetate
CAS-2624-43-3
ciclofenil
4-((4-(acetyloxy)phenyl)(cyclohexylidene)methyl)phenyl acetate
UNII-J468V64WZ1
p-Cresol, diacetate
Cyclofenil (Standard)
4-(Cyclohexylidenemethylene)-bis-phenol
4,4'-(Cyclohexylidenemethylene)bisphenol 1,1'-Diacetate
4-((4-(Acetyloxy)phenyl)cyclohexylidenemethyl)phenol Acetate
Bis(p-acetoxyphenyl)cyclohexylidenemethane
Cyclofenil (JAN/INN)
NCIOpen2_009345
SCHEMBL132246
CHEMBL141305
(cyclohexylidenemethanediyl)dibenzene-4,1-diyl diacetate
CHEBI:31446
G03GB01
GVOUFPWUYJWQSK-UHFFFAOYSA-N
BCP29796
Cyclofenil,4,4'-(Cyclohexylidenemethylene)bisphenol1,1'-diacetate
HY-W011100R
NSC86464
Tox21_112259
BDBM50523931
MFCD00190153
s5393
AKOS015900207
Tox21_112259_1
CCG-268218
CS-W011816
DB13472
FC20687
HY-W011100
NCGC00165767-01
NCGC00165767-03
NCGC00165767-04
AC-22576
AS-69834
Cyclofenil, >=98% (HPLC), white solid
DB-046909
NS00021958
C74360
D01281
Cyclophenil; F 6066; F6066;F-6066;Ondogyne
Q513583
SR-01000944933
SR-01000944933-1
BRD-K68996996-001-01-7
Cyclofenil,4,4\'-(Cyclohexylidenemethylene)bisphenol1,1\'-diacetate
Phenol, 4-((4-(acetyloxy)phenyl)cyclohexylidenemethyl)-, acetate (9CI)
220-089-1
4,4'-(Cyclohexylidenemethylene)bisphenol 1,1'-diacetate;4,4'-(Cyclohexylidenemethylene)diphenol diacetate ester
Solubility of 4-[(4-acetoxyphenyl)-cyclohexylidene-methyl]phenyl acetate (C26H28O4)
The solubility of 4-[(4-acetoxyphenyl)-cyclohexylidene-methyl]phenyl acetate in various solvents is influenced by its unique chemical structure, which includes both hydrophobic and hydrophilic characteristics. Understanding the solubility of this compound is crucial for its application in various fields, including pharmaceuticals and materials science. Here are some key considerations:
In general, while 4-[(4-acetoxyphenyl)-cyclohexylidene-methyl]phenyl acetate can be expected to dissolve moderately well in organic solvents such as ethyl acetate and chloroform, its solubility may be quite limited in aqueous environments. Understanding these solubility characteristics can help in applications where efficient dissolution is required.