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Amurensin

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Identification
Molecular formula
C16H13NO3
CAS number
53902-12-4
IUPAC name
2-(2-amino-3-methoxy-phenyl)chromen-4-one
State
State

At room temperature, Amurensin exists as a solid. It is typically stable under standard conditions if stored in a cool, dry place and protected from light.

Melting point (Celsius)
247.00
Melting point (Kelvin)
520.15
Boiling point (Celsius)
595.70
Boiling point (Kelvin)
868.85
General information
Molecular weight
283.28g/mol
Molar mass
283.2960g/mol
Density
1.3090g/cm3
Appearence

This compound typically appears as a crystalline solid. It may be encountered in a range of colors from off-white to pale yellow, depending on its purity and specific crystallization conditions. The compound may also be available as a powder or crystals.

Comment on solubility

Solubility of 2-(2-amino-3-methoxy-phenyl)chromen-4-one (C16H13NO3)

The solubility of 2-(2-amino-3-methoxy-phenyl)chromen-4-one can be quite intriguing. Here are several factors to consider:

  • Polarity: Its structure features both polar (amine and methoxy groups) and non-polar components, suggesting variable solubility in different solvents.
  • Solvent Interaction: This compound may exhibit better solubility in organic solvents such as ethanol or DMSO, rather than in water due to limited hydrogen bonding capabilities.
  • Temperature Effect: Generally, solubility increases with temperature; thus, heating might enhance its dissolution.

It's worth noting that certain structural attributes play a significant role in solubility behavior. For instance:

  1. The presence of the chromen-4-one moiety can influence its aromatic properties.
  2. The amino group can provide charged interactions in solution.
  3. The methoxy group can increase solubility through dipole interactions.

In conclusion, while the solubility profile of C16H13NO3 may not be straightforward, understanding the underlying factors can present a clearer picture of how this compound behaves in various solvents. Experimentation and empirical measurements are often the best ways to determine actual solubility in specific conditions.

Interesting facts

Interesting Facts about 2-(2-amino-3-methoxy-phenyl)chromen-4-one

2-(2-amino-3-methoxy-phenyl)chromen-4-one, also known as a flavonoid derivative, is a fascinating compound that presents a variety of intriguing attributes:

  • Flavonoid Family: This compound belongs to the flavonoid class, well-known for their antioxidant properties. Flavonoids play a crucial role in protecting cells from oxidative stress.
  • Biological Significance: Research has suggested that flavonoids like this one can exhibit significant health benefits, including anti-inflammatory, antitumor, and antibacterial activities. Their influence on human health is a promising area of study.
  • Novel Applications: Compounds similar to 2-(2-amino-3-methoxy-phenyl)chromen-4-one have been investigated for use in pharmaceuticals. They may contribute to developing new medications targeting various diseases.
  • Versatile Chemistry: The unique structure, characterized by a chromone backbone and an amine side group, allows for a multitude of potential modifications, paving the way for the synthesis of various derivatives with tailored biological activity.
  • Potential as Dyes: Beyond their biological applications, flavonoids may also serve as natural dyes in textiles and food products, providing vibrant colors derived from organic sources.

As a scientist or chemistry enthusiast delving into the world of flavonoids, one cannot help but be captivated by the multifaceted roles of compounds like 2-(2-amino-3-methoxy-phenyl)chromen-4-one. They bridge the gap between chemistry and biology, showcasing the beauty and complexity of molecular interactions.

Quote to Ponder: "Chemistry is the study of matter, but I prefer to view it as the study of change." – Isaac Asimov

Synonyms
167869-21-8
PD98059
PD 98059
2-(2-amino-3-methoxyphenyl)-4H-chromen-4-one
PD-98059
2-(2-Amino-3-methoxyphenyl)-4H-1-benzopyran-4-one
2-(2-amino-3-methoxyphenyl)chromen-4-one
PD 98,059
4H-1-Benzopyran-4-one, 2-(2-Amino-3-methoxyphenyl)-
2'-AMINO-3'-METHOXYFLAVONE
PD-098059
MFCD00671789
CHEBI:77954
C16H13NO3
UNII-SJE1IO5E3I
SJE1IO5E3I
NSC 679829
NSC-679828
CHEMBL35482
DTXSID40168416
2-(2'-amino-3'-methoxyphenyl)oxanaphthalen-4-one
PD 98059 [WHO-DD]
NSC679828
NSC-679829
2-(2-Amino-3-methoxy-phenyl)-chromen-4-one
SR-01000076097
PD 098059
2-(2-Amino-3-methoxyphenyl)-chromen-4-one
Tocris-1213
PD098059
Lopac-P-215
BiomolKI_000001
2-(2-amino-3-methoxy-phenyl)chromen-4-one
BiomolKI2_000011
PD 98,059, solid
Lopac0_001028
BMK1-B1
BSPBio_000996
KBioGR_000336
KBioSS_000336
MLS006010134
SCHEMBL157826
GTPL5241
2''-amino-3''-methoxyflavone
DTXCID1090907
BCBcMAP01_000049
KBio2_000336
KBio2_002904
KBio2_005472
KBio3_000671
KBio3_000672
BCPP000123
Bio1_000475
Bio1_000964
Bio1_001453
Bio2_000338
Bio2_000818
GLXC-04689
HMS1362B17
HMS1792B17
HMS1990B17
HMS3229M08
HMS3263M17
HMS3267D03
HMS3403B17
HMS3412O09
HMS3649N14
HMS3654I16
HMS3676O09
MEK INHIBITOR PD-98059
BCP02423
EX-A2127
Tox21_501028
BDBM50108771
HB2244
s1177
2-(2-Amino-3-methoxyphenyl)chromone
AKOS015995212
BCP9001060
BP34124
CCG-100605
CS-0169
LP01028
NSC 679828
SB16629
SDCCGSBI-0051000.P003
SDCCGSBI-0051000.P009
IDI1_002093
SMP2_000052
NCGC00015790-01
NCGC00015790-02
NCGC00015790-03
NCGC00015790-04
NCGC00015790-05
NCGC00015790-06
NCGC00015790-07
NCGC00015790-08
NCGC00025045-01
NCGC00025045-02
NCGC00025045-03
NCGC00025045-04
NCGC00025045-05
NCGC00179347-01
NCGC00261713-01
AC-28412
AS-19374
HY-12028
NCI60_028554
SMR001456459
SY052749
PD 98059?
A2529
EU-0101028
P-215
SW218254-2
P-4313
PD 98059 & Z-100
SR-01000076097-1
SR-01000076097-3
SR-01000076097-6
2-(2-amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran
BRD-K62810658-001-05-6
BRD-K62810658-001-06-4
BRD-K62810658-001-11-4
BRD-K62810658-001-12-2
BRD-K62810658-001-15-5
Q27088281
2-(2-Amino-3-methoxy-phenyl)-chromen-4-one(PD98059)
PD 98059 - CAS 167869-21-8
4H-1-Benzopyran-4-one, 2-(2-amino-3-methoxyphenyl)- & Z-100