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Xanthyletin

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Identification
Molecular formula
C15H12O5
CAS number
521-65-3
IUPAC name
4,9-dimethoxy-7-methyl-furo[3,2-g]chromen-5-one
State
State
At room temperature, Xanthyletin is typically found as a solid, characterized by its crystalline form, reflecting its orderly molecular arrangement.
Melting point (Celsius)
174.00
Melting point (Kelvin)
447.00
Boiling point (Celsius)
480.00
Boiling point (Kelvin)
753.00
General information
Molecular weight
268.26g/mol
Molar mass
268.2660g/mol
Density
1.3647g/cm3
Appearence

Xanthyletin is an off-white crystalline powder known for its unique structural properties due to the fusion of furan and chromen rings with methoxy and methyl functional groups.

Comment on solubility

Solubility of 4,9-Dimethoxy-7-methyl-furo[3,2-g]chromen-5-one (C15H12O5)

The solubility of 4,9-dimethoxy-7-methyl-furo[3,2-g]chromen-5-one is an intriguing aspect of this compound that can significantly influence its applications and behavior in various environments. Here are some key considerations regarding its solubility:

  • Solvent Compatibility: This compound is likely to be more soluble in organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO) due to the presence of multiple methoxy groups that enhance its polar characteristics.
  • Aqueous Solubility: It may exhibit limited solubility in water due to its hydrophobic furochromone structure, which can hinder interactions with water molecules.
  • Temperature Dependence: As with many organic compounds, its solubility can be temperature-dependent. Increased temperatures often promote higher solubility in solvents.
  • pH Influence: The solubility may also be affected by the pH of the solution, particularly if any of the hydroxyl groups ionize under acidic or basic conditions.

In summary, understanding the solubility of 4,9-dimethoxy-7-methyl-furo[3,2-g]chromen-5-one is crucial for researchers looking to utilize this compound in biological or chemical systems. As the old saying goes, "Like dissolves like," which reminds us to carefully choose solvents appropriate for optimal solubility.

Interesting facts

Interesting Facts about 4,9-Dimethoxy-7-methyl-furo[3,2-g]chromen-5-one

4,9-Dimethoxy-7-methyl-furo[3,2-g]chromen-5-one is a fascinating compound with various implications in the fields of chemistry and biology. This compound falls under the broader class of flavonoids, which are known for their diverse biological activities and health benefits.

Structural Characteristics

  • This compound features a unique fused ring system, combining elements of both furan and chromone structures, which contributes to its interesting chemical reactivity.
  • The presence of methoxy groups at the 4 and 9 positions plays a significant role in its chemical behavior and stability, potentially enhancing its solubility in organic solvents.

Biological Significance

Research has indicated that compounds related to flavonoids often exhibit various biological properties, including:

  • Antioxidant Activities: These compounds can help neutralize harmful free radicals in the body.
  • Anti-inflammatory Effects: Many flavonoids have demonstrated capabilities to reduce inflammation.
  • Neuroprotective Properties: Some studies suggest that flavonoids may offer protection to neural cells, enhancing brain health.

Applications in Research

This compound demonstrates potential applications in:

  • Natural Product Chemistry: It serves as a valuable compound for studying the interactions between natural products and biological systems.
  • Drug Development: Owing to its biological activities, it may inspire new pharmaceutical compounds or serve as leads in drug discovery.

Quote to Inspire

As the renowned chemist Marie Curie once said, "Nothing in life is to be feared, it is only to be understood." This statement rings true when we explore the depths of compounds like 4,9-dimethoxy-7-methyl-furo[3,2-g]chromen-5-one and their multifaceted roles in nature and health.

In summary, 4,9-dimethoxy-7-methyl-furo[3,2-g]chromen-5-one offers a multitude of opportunities for discovery and innovation in both scientific research and practical applications.

Synonyms
khellin
82-02-0
Visammin
Methafrone
Viscardan
Coronin
Amicardine
Ammivisnagen
Amikellin
Ammipuran
Benecardin
Corafurone
Gynokhellan
Kelourin
Khelloyd
Medekellin
Rykellin
Ammivin
Kelamin
Ammispasmin
Interkellin
Interkhellin
Kelicorin
Khelangin
Khellamine
Khellanals
Khellinorm
Visammimix
Visnagalin
Kalangin
Kelincor
Norkel
Simeskellina
Kellosal
Khelfren
Khelisem
Lynamine
Mefurina
Vasokellina
Visnagen
Amiptan
Chellin
Kelicor
Kellin
Kellina
Keloid
Eskel
Cardio-khellin
Ammi-khellin
Bi-Kellina
Benekardin
Khelline
Khelline I
Chellina
Khellinum
Quelina
4,9-Dimethoxy-7-methyl-5H-furo[3,2-g]chromen-5-one
Ammicardine
5,8-Dimethoxy-2-methyl-6,7-furanochromone
4,9-Dimethoxy-7-methyl-5H-furo(3,2-g)(1)benzopyran-5-one
4,9-Dimethoxy-7-methyl-5-oxofuro(3,2-g)-1,2-chromene
5,8-Dimethoxy-2-methyl-4',5'-furo-6,7-chromone
IT-033
kelina
CHEBI:6133
Viscardin
5H-Furo[3,2-g][1]benzopyran-5-one, 4,9-dimethoxy-7-methyl-
5,8-Dimethoxy-2-methyl-4',5'-furano-6,7-chromone
EINECS 201-392-8
UNII-5G117T0TJZ
MFCD00005007
NSC 25509
NSC 37744
NSC-25509
NSC-37744
4,9-Dimethoxy-7-methyl-5-oxo-1,8-dioxabenz-(f)indene
4,9-Dimethoxy-7-methyl-5-oxofuro(3,2-g)(1)benzopyran
BRN 0263185
5G117T0TJZ
4,9-dimethoxy-7-methylfuro[3,2-g]chromen-5-one
5H-Furo(3,2-g)(1)benzopyran-5-one, 4,9-dimethoxy-7-methyl-
DTXSID9045267
AI3-52114
NSC37744
Chorafurone
Vismagen
Khell
MLS000028448
DTXCID7025267
4,9-Dimethoxy-7-methyl-5H-furo[3,2-g]-[1]benzopyran-5-one
4,9-Dimethoxy-7-methyl-5H-furo[3,2-g][1]benzopyran-5-one
NSC8519
5-19-06-00320 (Beilstein Handbook Reference)
5,7-furanochromone
CAS-82-02-0
NCGC00016327-01
SMR000058278
4,2-g][1]benzopyran
KHELLIN (MART.)
KHELLIN [MART.]
4,8-dioxabenz-[f]indene
4,2-g]-1,2-chromene
5,5'-furo-6,7-chromone
5,5'-furano-6,7-chromone
Chellina [Italian]
4,2-g][1]benzopyran-5-one
Khellin [INN:DCF]
Khelline [INN-French]
Khellinum [INN-Latin]
Quelina [INN-Spanish]
5H-Furo[3, 4,9-dimethoxy-7-methyl-
WLN: T C566 DO JV MOJ BO1 HO1 L1
SR-01000000072
4,9-dimethoxy-7-methyl-5H-furo(3,2-g)chromen-5-one
Gynokhellin
Intercellin
Hkelfren
Prestwick_287
Spectrum_000079
Khellin, for microscopy
Opera_ID_372
KHELLIN [INN]
KHELLIN [MI]
Prestwick0_000091
Prestwick1_000091
Prestwick2_000091
Prestwick3_000091
Spectrum2_000593
Spectrum3_000654
Spectrum4_001557
Spectrum5_000154
KHELLIN [WHO-DD]
bmse000751
SCHEMBL9655
Khellin, analytical standard
BSPBio_000042
BSPBio_002287
KBioGR_002054
KBioSS_000479
SPECTRUM210866
MLS001076533
CHEMBL44746
DivK1c_000046
5,9-dimethoxy-2-methylfurano[3,2-g]chromen-4-one
SPBio_000466
SPBio_001981
BPBio1_000048
MEGxp0_000331
ACon0_000983
ACon1_000350
HMS500C08
HSMPDPBYAYSOBC-UHFFFAOYSA-
KBio1_000046
KBio2_000479
KBio2_003047
KBio2_005615
KBio3_001507
NINDS_000046
HMS1568C04
HMS1923M07
HMS2095C04
HMS2230B16
HMS3371C21
HMS3712C04
Pharmakon1600-00210866
ALBB-025052
HY-B1394
NSC-8519
NSC25509
Tox21_110374
BDBM50480260
CCG-36453
LMPK13110001
NSC755826
s5887
STL561007
AKOS002281934
Tox21_110374_1
FK52456
NSC-755826
SDCCGMLS-0003040.P003
IDI1_000046
NCGC00016327-02
NCGC00016327-03
NCGC00016327-04
NCGC00016327-05
NCGC00016327-06
NCGC00016327-07
NCGC00016327-08
NCGC00016327-09
NCGC00016327-11
NCGC00023424-03
NCGC00023424-04
NCGC00169160-01
NCGC00169160-02
NCGC00169160-03
AS-35307
DA-54630
SY051635
SBI-0051567.P002
CS-0013121
K0039
NS00005943
C09010
AB00052134_16
AK-693/40760628
4,9-Dimethoxy-7-methyl-furo[3,2-g]chromen-5-one
Q2079998
SR-01000000072-3
SR-01000000072-4
SR-01000000072-5
SR-01000000072-6
BRD-K80353807-001-05-5
BRD-K80353807-001-06-3
BRD-K80353807-001-16-2
BRD-K80353807-001-24-6
BRD-K80353807-001-25-3
4,9-dimethoxy-7-methylpyrano[3,2-f][1]benzoxol-5-one
4,9-Dimethoxy-7-methyl-5H-furo[3,2-g]chromen-5-one #
201-392-8
InChI=1/C14H12O5/c1-7-6-9(15)10-11(16-2)8-4-5-18-12(8)14(17-3)13(10)19-7/h4-6H,1-3H3