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Coumarin

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Identification
Molecular formula
C9H6O2
CAS number
91-64-5
IUPAC name
1,2-dihydrobenzo[f]chromen-3-one
State
State

At room temperature, coumarin is in a solid state. Its crystalline structure and aromatic properties make it noticeable even at this state.

Melting point (Celsius)
70.00
Melting point (Kelvin)
343.00
Boiling point (Celsius)
301.00
Boiling point (Kelvin)
574.00
General information
Molecular weight
146.15g/mol
Molar mass
146.1440g/mol
Density
0.9350g/cm3
Appearence

Coumarin is a crystalline compound that is colorless to white. It often takes a needle-like crystal form and has a sweet, vanilla-like aroma. This fragrance is one of its distinguishing properties, and coumarin is frequently used in perfumes and flavorings for its scent profile.

Comment on solubility

Solubility of 1,2-dihydrobenzo[f]chromen-3-one (C9H6O2)

1,2-dihydrobenzo[f]chromen-3-one is a fascinating compound that exhibits variable solubility characteristics. Understanding its solubility behavior is essential for applications in various chemical processes. Here are some key points about its solubility:

  • Solvent Dependency: The solubility of C9H6O2 is significantly influenced by the choice of solvent. It tends to dissolve well in organic solvents such as ethanol, dichloromethane, and acetone.
  • Limited Water Solubility: This compound shows poor solubility in water, which is characteristic of many organic compounds with aromatic structures.
  • Temperature Variation: Solubility can also vary with temperature. Generally, an increase in temperature may enhance the solubility in organic solvents.

In summary, while 1,2-dihydrobenzo[f]chromen-3-one is not very soluble in water, it displays favorable solubility in various organic solvents, making it a compound of interest for organic syntheses and applications in chemical research.

Interesting facts

Interesting Facts About 1,2-Dihydrobenzo[f]chromen-3-one

1,2-Dihydrobenzo[f]chromen-3-one is a fascinating compound that showcases the rich diversity of organic chemistry. This compound is known for its polycyclic structure, which consists of a fused benzo and chromenone ring system. Here are some compelling facts about this interesting molecule:

  • Structural Diversity: The unique fusion of benzene and chromenone rings allows for a wide range of derivatives, which can exhibit various biological activities.
  • Pharmacological Potential: Compounds of this class are often investigated for their potential as antioxidants, anti-inflammatory agents, and even anticancer agents. This positions them as valuable targets in medicinal chemistry.
  • Natural Occurrence: Some derivatives of this compound can be derived from naturally occurring sources, further emphasizing the interconnectedness of organic compounds and nature.
  • Research Relevance: Ongoing research is being conducted to explore the full potential of 1,2-dihydrobenzo[f]chromen-3-one in various applications, including drug development and the synthesis of novel materials.

As noted in a recent study, “the exploration of this compound's derivatives can pave the way for breakthroughs in healthcare.” This statement underscores the importance of fundamental research in unlocking the myriad possibilities that lie within such a simple-looking structure.

In summary, 1,2-dihydrobenzo[f]chromen-3-one exemplifies the relationship between structure and function in chemistry and biology. Its intriguing characteristics not only contribute to academic research but also hold promise for practical applications in the pharmaceutical industry.

Synonyms
splitomicin
5690-03-9
Splitomycin
1,2-Dihydro-3H-naphtho[2,1-b]pyran-3-one
1,2-dihydro-3h-benzo[f]chromen-3-one
1,2-dihydrobenzo[f]chromen-3-one
CHEMBL86537
CHEBI:75272
DTXSID201017436
MFCD08705254
3H-Naphtho[2,1-b]pyran-3-one, 1,2-dihydro-
1H-benzo[f]chromen-3(2H)-one
1,2-Dihydro-3H-naphtho(2,1-b)pyran-3-one
Bio2_000878
Tocris-1542
1H,2H,3H-naphtho[2,1-b]pyran-3-one
1-Naphthalen propanoic acid
BSPBio_001116
KBioGR_000456
KBioSS_000456
GTPL8101
SCHEMBL2544804
BDBM29590
KBio2_000456
KBio2_003024
KBio2_005592
KBio3_000851
KBio3_000852
ISFPDBUKMJDAJH-UHFFFAOYSA-N
Bio2_000398
DTXCID201475632
HMS1362H17
HMS1792H17
HMS1990H17
HMS3268C11
HMS3403H17
HMS3412J05
HMS3676J05
BCP10432
HB4091
s7593
Splitomicin - CAS 5690-03-9
AKOS006288326
CCG-208679
Splitomicin, >=98% (HPLC), powder
IDI1_002153
NCGC00025208-01
NCGC00025208-02
NCGC00025208-03
NCGC00025208-05
AC-35443
AS-56331
DA-58051
HY-100585
CS-0019737
S0892
1,2-dihydro-3H-naphtho[2,1-b]-pyran-3-one
T72636
SR-01000597607
SR-01000597607-1
BRD-K27710560-001-02-6
BRD-K27710560-001-07-5
Q27088853
1-Naphthalenepropionic acid, 2-hydroxy-, .delta.-lactone