Skip to main content

Psoralen

ADVERTISEMENT
Identification
Molecular formula
C11H6O3
CAS number
66-97-7
IUPAC name
furo[3,2-g]chromen-7-one
State
State

Psoralen is a solid at room temperature. It is known for its crystalline structure.

Melting point (Celsius)
152.00
Melting point (Kelvin)
425.15
Boiling point (Celsius)
410.00
Boiling point (Kelvin)
683.15
General information
Molecular weight
186.16g/mol
Molar mass
186.1620g/mol
Density
1.5650g/cm3
Appearence

Psoralen appears as colorless or white crystals. It is a solid compound at room temperature and is notably used in various dermatological treatments.

Comment on solubility

Solubility of Furo[3,2-g]chromen-7-one

The solubility of furo[3,2-g]chromen-7-one (C11H6O3) can be influenced by several factors, such as temperature and the presence of different solvents. Here are some key points to consider regarding its solubility:

  • Solvent Polarity: Furo[3,2-g]chromen-7-one tends to have better solubility in organic solvents that are non-polar or slightly polar.
  • Temperature Dependency: Like many organic compounds, its solubility may increase with temperature, making it more soluble in warmer solvents.
  • Hydrophilicity vs Hydrophobicity: The presence of >C=O (carbonyl) groups suggests a degree of polarity, which can allow for limited solubility in polar solvents such as ethanol or methanol.
  • Crystalline Form: The crystalline structure of furo[3,2-g]chromen-7-one can affect solubility; finer crystals often dissolve more easily than larger, bulkier ones.

In conclusion, while furo[3,2-g]chromen-7-one exhibits variable solubility depending on solvent and conditions, it is often recommended to test its solubility in different environments for optimal use in applications.

Interesting facts

Explore the Fascinating World of Furo[3,2-g]chromen-7-one

Furo[3,2-g]chromen-7-one, a unique compound belonging to the class of chromones, offers a delightful insight into the realms of organic chemistry and its applications. Here are some intriguing aspects of this compound:

  • Natural Occurrence: Furo[3,2-g]chromen-7-one is often found in various plants, contributing to their coloration and aroma. This compound may play a significant role in the ecological interactions between plants and their environments.
  • Biological Activity: Research has highlighted the potential biological activities of furo[3,2-g]chromen-7-one, including antioxidant and anti-inflammatory properties. These qualities make it a compound of interest in medicinal chemistry.
  • Versatile Applications: Beyond its natural occurrence, furo[3,2-g]chromen-7-one can be synthesized for use in various industries, including pharmaceuticals and agrochemicals. Scientists are exploring its utility in developing effective drug formulations.
  • Structure-Activity Relationship: The unique furochromene structure allows researchers to investigate the relationship between its molecular features and biological activity. This plays a critical role in the design of novel compounds with enhanced efficacy.

As a compound with rich potential, furo[3,2-g]chromen-7-one exemplifies the intersection of nature and chemistry. Its fascinating properties beckon further exploration, promising discoveries that may benefit both science and society. In the words of renowned chemist Linus Pauling, "Chemistry is the study of the structure, properties, and reactions of matter." Furo[3,2-g]chromen-7-one embodies these elements, making it a worthy subject of study.

Synonyms
Psoralen
66-97-7
7H-Furo[3,2-g]chromen-7-one
Ficusin
Furocoumarin
Psoralene
7H-Furo[3,2-g][1]benzopyran-7-one
Psorline-P
furo[3,2-g]chromen-7-one
6,7-Furanocoumarin
Furo(3,2-g)-coumarin
Furo(2',3',7,6)coumarin
Furo(4',5',6,7)coumarin
Furo[3,2-g]coumarin
NSC 404562
CCRIS 4343
Manaderm
Furo[2',3':7,6]coumarin
Furo[4',5':6,7]coumarin
KTZ7ZCN2EX
UNII-KTZ7ZCN2EX
7H-Furo(3,2-g)(1)benzopyran-7-one
HSDB 3528
7H-Furo[3,2-g]benzopyran-7-one
EINECS 200-639-7
6-Hydroxy-5-benzofuranacrylic acid beta-lactone
NSC-404562
BRN 0152784
Furo[2'.3':7.6]coumarin
5-Benzofuranacrylic acid, 6-hydroxy-, delta-lactone
CHEBI:27616
MFCD00010520
6-hydroxy-5-benzofuranacrylic acid delta-lactone
CHEMBL164660
2H-furo[3,2-g]chromen-2-one
2-Propenoic acid, 3-(6-hydroxy-5-benzofuranyl)-, delta-lactone
DTXSID00216205
6-hydroxy-5-benzofuranacrylic acid gamma-lactone
5-19-04-00445 (Beilstein Handbook Reference)
TNP00293
Psoralen (Ficusin)
3-(6-hydroxy-5-benzofuranyl)-2-propenoic acid delta-lactone
PSORALEN (USP-RS)
PSORALEN [USP-RS]
furo(2',3':7,6)coumarin
furo(4',5':6,7)coumarin
7H-Furo(3,2-g)chromen-7-one
C11H6O3
furo
furano[3,2-g]chromen-2-one
Psoralene (DCF)
Manaderm (TN)
Psoralen,(S)
Psoralen (Standard)
Psoralen, 97%
Furo[4',7]coumarin
PHYTOALEXIN-CMPD
PSORALEN [HSDB]
PSORALEN [MI]
PSORALEN [WHO-DD]
Oprea1_841692
SCHEMBL17835
Psoralen, analytical standard
MLS001304059
MEGxp0_001172
Psoralen, >=99% (HPLC)
ACon1_001579
HY-N0053R
pyrano[5,6-f]benzofuran-7-one
DTXCID60138696
HMS2267L05
BCP04177
HY-N0053
7H-Furo[3,2-g]chromen-7-one #
BDBM50331544
NSC404562
s4737
STL564822
AKOS004110987
AC-7968
CCG-266472
CS-3756
FP15273
FURO(2',3':7',6)COUMARIN
NCGC00017351-01
NCGC00017351-02
NCGC00017351-03
NCGC00017351-07
NCGC00142529-01
AS-59034
SMR000112587
NS00015842
P2077
7H-Furo[3,2-g][1]benzopyran-7-one, 9CI
6-hydroxy-5-benzofuranacrylic Acid deta-lacton
C09305
D08450
AA-504/20833002
AJ-738/21166005
Q417788
BRD-K47264279-001-01-4
BRD-K47264279-001-08-9
5-Benzofuranacrylic acid, 6-hydroxy-, .delta.-lactone
Z1201617131
6-HYDROXY-5-BENZOFURANACRYLIC ACID .DELTA.-LACTONE
2-Propenoic acid, 3-(6-hydroxy-5-benzofuranyl)-, .delta.-lactone
InChI=1/C11H6O3/c12-11-2-1-7-5-8-3-4-13-9(8)6-10(7)14-11/h1-6
200-639-7