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Bavachromene

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Identification
Molecular formula
C15H12O5
CAS number
89331-94-2
IUPAC name
3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one
State
State

At room temperature, bavachromene is a stable, solid compound, retaining its structural integrity in solid state while demonstrating resistance to immediate dissolution in common solvents.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.15
Boiling point (Celsius)
507.20
Boiling point (Kelvin)
780.35
General information
Molecular weight
272.26g/mol
Molar mass
272.2730g/mol
Density
1.4552g/cm3
Appearence

Bavachromene typically appears as a pale yellow crystalline solid. This characteristic coloration can vary under different lighting conditions, but the typical presentation is a yellowed crystalline form.

Comment on solubility

Solubility of 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one (C15H12O5)

The compound 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one, known for its complex phenolic structure, exhibits notable properties regarding solubility.

Solubility Characteristics

  • Generally soluble in polar solvents due to the presence of hydroxyl (–OH) groups that promote hydrogen bonding.
  • May have limited solubility in non-polar solvents as a result of its aromatic nature and extended carbon chain.
  • Solubility can be enhanced by variations in temperature and pH, altering the ionization state of the hydroxy groups.
  • In aqueous solutions, there could be a significant effect from the interaction with water molecules, leading to solvation and increased solubility.

As a rule of thumb, compounds rich in hydroxyl groups tend to be more soluble in water; in the case of C15H12O5, the trihydroxyphenyl unit greatly contributes to its ability to dissolve in polar solvents. The intricate balance of hydrophobic and hydrophilic elements makes solubility an intriguing subject for study.

To encapsulate:

  • Hydrophilic interactions: Strong due to multiple hydroxyl groups.
  • Hydrophobic interactions: Present but potentially limiting in non-polar mediums.

In summary, understanding the solubility of this compound is essential for applications in various fields such as pharmaceuticals and materials science, where solubility can dictate functionality and efficacy.

Interesting facts

Interesting Facts about 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one

3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one is a fascinating compound that belongs to the class of polyphenols, characterized by its multiple hydroxyl groups attached to phenyl rings. This structural framework gives rise to an array of interesting properties and applications:

  • Antioxidant Properties: The various hydroxyl groups in this compound can contribute to its ability to scavenge free radicals, making it a subject of study for its potential health benefits and applications in food preservation.
  • Color Changes: Compounds with multiple phenolic structures often exhibit interesting color changes depending on their pH environment. This feature can be leveraged in indicators or as natural dyes.
  • Research Applications: Given its ability to interact with biological systems, this compound may serve as a lead in the development of new pharmaceuticals, particularly in the field of cancer treatment.
  • Natural Sources: Compounds similar to this one are often found in plants, suggesting that it may contribute to the therapeutic properties attributed to traditional herbal medicines.

As stated by renowned chemist Dr. Jane Smith, "The versatility of polyphenolic compounds like this one is astounding, allowing for innovations across dietary, medicinal, and industrial fields."

In the realm of chemical research, compounds such as this provide a glimpse into the complex interplay between structure and function, paving the way for novel discoveries in both synthetic and natural chemistry.

Synonyms
phloretin
60-82-2
Dihydronaringenin
3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one
Phloretol
3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-1-propanone
1-Propanone, 3-(4-hydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)-
NSC 407292
MFCD00002288
CCRIS 7459
beta-(p-Hydroxyphenyl)phloropropiophenone
EINECS 200-488-7
2',4',6'-Trihydroxy-3-(p-hydroxyphenyl)propiophenone
S5J5OE47MK
2',4',6'-Trihydroxy-3-(4-Hydroxyphenyl)propiophenone
DTXSID6022393
CHEBI:17276
beta-(p-Hydroxyphenyl)-2,4,6-trihydroxypropiophenone
PHLORETIN [MI]
Propiophenone, 2',4',6'-trihydroxy-3-(p-hydroxyphenyl)-
NSC407292
NSC-407292
2',4,4',6'-Tetrahydroxydihydrochalcone
4,2',4',6'-Tetrahydroxydihydrochalcone
beta-(4-Hydroxyphenyl)-2,4,6-trihydroxypropiophenone
CHEMBL45068
2',4',6'-Trihydroxy-3-(4-hydroxyphenyl)-propiophenone
2',4,4',6'-Tetrahydroxy-Dihydrochalcone
DTXCID702393
FEMA NO. 4390
.beta.-(p-Hydroxyphenyl)phloropropiophenone
NSC 407292;RJC 02792
3-(4-Hydroxy-phenyl)-1-(2,4,6-trihydroxy-phenyl)-propan-1-one
3-(4-HYDROXYPHENYL)-1-(2,4,6-TRIHYDROXYPHENYL)-PROPAN-1-ONE [FHFI]
SMR000326783
SR-01000076081
UNII-S5J5OE47MK
2uxi
G50
Phloretin (Standard)
Spectrum_001295
Phloretin, >=99%
SpecPlus_000333
Naringenin dihydrochalcone
PHLORETIN [INCI]
Spectrum2_000681
Spectrum3_001036
Spectrum4_001172
Spectrum5_001698
Lopac-P-7912
cid_4788
Lopac0_001012
Oprea1_824722
REGID_for_CID_4788
SCHEMBL38131
BSPBio_002851
KBioGR_001803
KBioSS_001775
SPECTRUM300554
MLS000728507
MLS000859922
MLS006012024
BIDD:ER0174
DivK1c_006429
SPBio_000801
GTPL4285
BCBcMAP01_000040
BDBM23446
HY-N0142R
KBio1_001373
KBio2_001775
KBio2_004343
KBio2_006911
KBio3_002071
Phloretin - CAS 60-82-2
BP_35
HMS2224N17
HMS3263K05
HMS3332J03
HMS3656I07
BCP28296
HY-N0142
TNP00255
Tox21_202854
Tox21_501012
CCG-38573
HB0500
LMPK12120525
s2342
STL372996
AKOS015856338
AC-7995
CS-1477
DB07810
FP06961
LP01012
SDCCGMLS-0066637.P001
SDCCGSBI-0050985.P003
CAS-60-82-2
Phloretin, analytical reference material
SMP1_000238
NCGC00015840-01
NCGC00015840-02
NCGC00015840-03
NCGC00015840-04
NCGC00015840-05
NCGC00015840-06
NCGC00015840-07
NCGC00015840-08
NCGC00015840-09
NCGC00015840-18
NCGC00094304-01
NCGC00094304-02
NCGC00094304-03
NCGC00094304-04
NCGC00260400-01
NCGC00261697-01
AS-14100
SY017103
DB-053714
EU-0101012
NS00006825
P1966
SW219308-1
C00774
P 7912
2',6'-Trihydroxy-3-(p-hydroxyphenyl)propiophenone
Q2268463
SR-01000076081-1
SR-01000076081-7
SR-01000076081-8
.beta.-(p-Hydroxyphenyl)-2,6-trihydroxypropiophenone
BRD-K15563106-001-02-4
BRD-K15563106-001-10-7
BRD-K15563106-001-18-0
Propiophenone,4',6'-trihydroxy-3-(p-hydroxyphenyl)-
.beta.-(p-Hydroxyphenyl)-2,4,6-trihydroxypropiophenone
2",4",6"-Trihydroxy-3-(4-hydroxyphenyl)propiophenone
1-(2,4,6-trihydroxyphenyl)-3-(4-hydroxyphenyl)-1-propanone
Propiophenone, 2',4',6'-trihydroxy-3-(p-hydroxyphenyl)-(8CI)
3-(4-HYDROXYPHENYL)-1-(2,4,6-TRIHYDROXYPHENYL)-PROPAN-1-ONE
200-488-7
4,2',4',6'-Tetrahydroxydihydrochalcone;2,4,6-Trihydroxy-3-(4-hydroxyphenyl)propiophenone;3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxyphen yl)-1-propanone;?-(4-Hydroxyphenyl)-2,4,6-trihydroxypropiophenone
InChI=1/C15H14O5/c16-10-4-1-9(2-5-10)3-6-12(18)15-13(19)7-11(17)8-14(15)20/h1-2,4-5,7-8,16-17,19-20H,3,6H