Interesting facts
Interesting Facts about 1-(4-Hydroxy-3,5-Dimethoxy-Phenyl)Ethanone
1-(4-Hydroxy-3,5-dimethoxy-phenyl)ethanone, often referred to in the scientific community for its unique structure and properties, is a compound that has garnered significant attention for various reasons:
- Natural Product Derivative: This compound is a derivative of natural products, which means it can be found in or synthesized from natural sources. Many natural products are known for their medicinal properties, and derivatives like this one can enhance their efficacy.
- Medicinal Applications: Research has shown that compounds with similar structures often exhibit biological activities, including antioxidant, anti-inflammatory, and even anticancer properties. This makes 1-(4-hydroxy-3,5-dimethoxy-phenyl)ethanone a subject of interest in pharmacology.
- Synthetic Challenges: Chemists often find it intriguing to synthesize this compound due to the complexity involved in its positioning of functional groups. The hydroxy and methoxy groups can play crucial roles in the compound's chemical reactivity.
- Structure-Activity Relationship (SAR): Understanding how variations in the structure of this compound affect its biological activity helps researchers design more effective drugs. For instance, changing the position or nature of substituents on the aromatic ring can drastically alter how the compound interacts with biological targets.
- Cultural Relevance: The compound has also piqued the interest of those studying traditional medicine systems where similar compounds are used for therapeutic purposes, highlighting the intersection of chemistry and cultural practices.
In the words of chemist Robert H. Grubbs, "The challenge and beauty of chemistry lie in the connections we make and the properties we discover." This quote aptly encapsulates the journey into understanding 1-(4-hydroxy-3,5-dimethoxy-phenyl)ethanone, showcasing its potential in the realms of both innovation and nature.
Overall, this compound not only represents an exciting area of study in synthetic and medicinal chemistry, but it also plays a crucial role in bridging the gap between natural remedies and modern pharmacology.
Synonyms
Acetosyringone
2478-38-8
1-(4-Hydroxy-3,5-dimethoxyphenyl)ethanone
4'-HYDROXY-3',5'-DIMETHOXYACETOPHENONE
Ethanone, 1-(4-hydroxy-3,5-dimethoxyphenyl)-
Acetosyringenin
3,5-Dimethoxy-4-hydroxyacetophenone
1-(4-hydroxy-3,5-dimethoxyphenyl)ethan-1-one
Acetophenone, 4'-hydroxy-3',5'-dimethoxy-
CCRIS 7286
4-hydroxy-3,5-dimethoxyacetophenone
EINECS 219-610-5
4-Hydroksy-3',5'-dwumetoksyacetofenon
BRN 1966119
CHEBI:2404
Acetophenone, 3,5-dimethoxy-4-hydroxy-
4-Hydroksy-3',5'-dwumetoksyacetofenon [Polish]
866P45Y84S
DTXSID2062454
DTXCID1037147
4Hydroksy3',5'dwumetoksyacetofenon
3',5'Dimethoxy4'hydroxyacetophenone
4'Hydroxy3',5'dimethoxyacetophenone
1(4Hydroxy3,5dimethoxyphenyl)ethanone
Acetophenone, 4'hydroxy3',5'dimethoxy
Ethanone, 1(4hydroxy3,5dimethoxyphenyl)
Acetophenone, 4'hydroxy3',5'dimethoxy (8CI)
Acetophenone, 4'-hydroxy-3',5'-dimethoxy-(8CI)
Ethanone, 1-(4-hydroxy-3,5-dimethoxyphenyl)-(9CI)
219-610-5
3',5'-Dimethoxy-4'-hydroxyacetophenone
Acetosyringon
MFCD00008748
4-Hydroxy-3,5-dimethoxyacetophennone
4-acetylsyringol
UNII-866P45Y84S
Spectrum_001915
SpecPlus_000955
Spectrum2_000429
Spectrum3_001115
Spectrum4_001953
Spectrum5_000695
bmse000576
bmse010032
1-(4-Hydroxy-3,5-dimethoxy-phenyl)-ethanone
SCHEMBL15511
BSPBio_002850
KBioGR_002389
KBioSS_002457
SPECTRUM300610
MLS002207209
DivK1c_007051
4-acetyl-2,6-dimethoxyphenol
SPBio_000418
CHEMBL224146
KBio1_001995
KBio2_002450
KBio2_005018
KBio2_007586
KBio3_002070
Phenol, 4-acetyl-2,6-dimethoxy
BBL101364
CCG-39967
s4955
STL555160
AKOS005258861
3',5-Dimethoxy-4'-hydroxyacetophenone
CS-W010600
FD16078
HY-W009884
SDCCGMLS-0066948.P001
NCGC00095819-01
NCGC00095819-02
3', 5'-dimethoxy-4'-hydroxyacetophenone
MS-20205
SMR000112388
SY049152
DB-022069
D2666
NS00010763
1-(3,5-dimethoxy-4-oxidanyl-phenyl)ethanone
3',5'-Dimethoxy-4'-hydroxyacetophenone, 97%
4'-Hydroxy-3',5'-dimethoxyacetophenone, 97%
EN300-112111
F20446
3',5'-DIMETHOXY-4'-HYDROXY-ACETOPHENONE
A817490
Q906309
SR-05000002436
A1-00327
SR-05000002436-1
Acetosyringone;4'-Hydroxy-3',5'-dimethoxyacetophenone
BRD-K66643401-001-02-4
BRD-K66643401-001-04-0
Z1255450019
3 inverted exclamation marka,5 inverted exclamation marka-Dimethoxy-4 inverted exclamation marka-hydroxyacetophenone
4 inverted exclamation mark -Hydroxy-3 inverted exclamation mark ,5 inverted exclamation mark -dimethoxyacetophenone
InChI=1/C10H12O4/c1-6(11)7-4-8(13-2)10(12)9(5-7)14-3/h4-5,12H,1-3H
Solubility of 1-(4-hydroxy-3,5-dimethoxy-phenyl)ethanone
The solubility of 1-(4-hydroxy-3,5-dimethoxy-phenyl)ethanone is influenced by several factors due to its unique structural features. Here are some key points regarding its solubility:
Overall, the solubility profile of 1-(4-hydroxy-3,5-dimethoxy-phenyl)ethanone suggests moderate solubility in polar solvents while potentially offering better solubility in non-polar and less polar organic environments.
It's crucial to assess the specific conditions (such as temperature and pH) for practical applications since solubility can greatly influence the compound's behavior in different systems.