Interesting facts
Interesting Facts about 1-(2,4,6-trihydroxyphenyl)propan-1-one
1-(2,4,6-trihydroxyphenyl)propan-1-one, also known as a derivative of flavonoids, offers a fascinating insight into the world of chemistry due to its structural and functional uniqueness. This compound is notable for a variety of reasons:
- Biological Significance: This compound is a potential antioxidant, which means it can help combat oxidative stress in biological systems. Its ability to neutralize free radicals makes it an important subject of study in medicinal chemistry.
- Phenolic Structure: The presence of three hydroxyl groups on the aromatic ring enhances its reactivity and biological activity. Such phenolic compounds have been linked to numerous health benefits, including anti-inflammatory and anti-cancer properties.
- Applications: Beyond its biological significance, it has potential applications in the food and cosmetic industries as a natural preservative or as an ingredient in various formulations to enhance stability and provide color.
- Synthetic Pathways: The synthesis of 1-(2,4,6-trihydroxyphenyl)propan-1-one can provide insights into the broader category of phenolic compounds and their derivatives, showing how structural variations can lead to diverse chemical properties.
- Cultural Relevance: Compounds such as this have been used in traditional medicine for centuries, showcasing the long-standing relationship between chemistry and culture, particularly in healing practices.
In conclusion, the study of 1-(2,4,6-trihydroxyphenyl)propan-1-one represents a bridge between fundamental chemistry and practical applications, revealing how the unique properties of chemical compounds can impact various fields. As research continues, this compound may unveil even more exciting possibilities in the realms of health and industry.
Synonyms
flopropione
2295-58-1
2',4',6'-Trihydroxypropiophenone
1-(2,4,6-trihydroxyphenyl)propan-1-one
Cospanon
Phloropropiophenone
Argobyl
Phloropropionone
Propiophloroglucine
Chlonarin
Flopropion
Gasstenon
Labrodax
Supanate
Supazlun
Ecapron
Labroda
1-Propanone, 1-(2,4,6-trihydroxyphenyl)-
Labrodax supanate
Propionylphloroglucinol
Ephtanon
Flopropiona
2,4,6-Trihydroxypropiophenone
Flopropionum
1-(2,4,6-Trihydroxyphenyl)-1-propanone
Flopropionum [INN-Latin]
Flopropiona [INN-Spanish]
RP 13907
Flopropione [INN:DCF:JAN]
NSC 97909
EINECS 218-942-8
13907 R. P.
NSC-97909
Ephtanon (TN)
PROPIOPHENONE, 2',4',6'-TRIHYDROXY-
BRN 2096799
05V5NVB5Y1
DTXSID3045851
AI3-36955
FLOPROPIONE [MI]
FLOPROPIONE [INN]
FLOPROPIONE [JAN]
FLOPROPIONE [MART.]
FLOPROPIONE [WHO-DD]
13907 R.P.
DTXCID1025851
3-08-00-03413 (Beilstein Handbook Reference)
NCGC00094817-01
Flopropionum (INN-Latin)
Flopropiona (INN-Spanish)
FLOPROPIONE (MART.)
Profenon
CAS-2295-58-1
UNII-05V5NVB5Y1
Gallepronin
Flopion
Spamorin
Spasmoril
Pasmus
Phlopropiophenone
propanoyl-phloroglucinol
Spectrum_000563
Spectrum2_000954
Spectrum3_000579
Spectrum4_000391
Spectrum5_001471
Flopropione (JP17/INN)
2,6-Trihydroxypropiophenone
SCHEMBL26316
BSPBio_001998
KBioGR_000941
KBioSS_001043
DivK1c_000482
SPECTRUM1500629
SPBio_000948
2',6'-Trihydroxypropiophenone
CHEMBL1605835
CHEBI:31614
HMS501I04
KBio1_000482
KBio2_001043
KBio2_003611
KBio2_006179
KBio3_001498
NINDS_000482
Propiophenone,4',6'-trihydroxy-
HMS1921M05
HMS3652F21
HMS3885N13
Pharmakon1600-01500629
NSC97909
Tox21_111340
CCG-40074
MFCD00016456
NSC757392
s4249
AKOS016357612
Tox21_111340_1
CS-8184
FT70412
NSC-757392
IDI1_000482
NCGC00094817-02
NCGC00094817-03
NCGC00094817-05
AC-32766
SBI-0051564.P002
DB-019834
HY-100562
NS00027311
SW219253-1
T0887
D01259
D83820
AB00052131_02
SR-01000872776
Q5460218
SR-01000872776-1
BRD-K43383936-001-02-9
BRD-K43383936-001-04-5
BRD-K43383936-001-05-2
218-942-8
InChI=1/C9H10O4/c1-2-6(11)9-7(12)3-5(10)4-8(9)13/h3-4,10,12-13H,2H2,1H
Solubility of 1-(2,4,6-trihydroxyphenyl)propan-1-one (C9H8O4)
The solubility of 1-(2,4,6-trihydroxyphenyl)propan-1-one, commonly referred to for its unique structure, is intriguing due to its functional groups. Understanding its solubility can be approached by examining the following factors:
In summary, 1-(2,4,6-trihydroxyphenyl)propan-1-one is likely to exhibit good solubility in polar solvents, while its solubility in non-polar solvents may be limited due to its structural features. Understanding these nuances is essential for applications in various fields, including pharmaceuticals and material sciences.