Skip to main content

(4-methyl-2-oxo-coumarin-7-yl) acetate

ADVERTISEMENT
Identification
Molecular formula
C13H10O4
CAS number
88237-12-3
IUPAC name
(4-methyl-2-oxo-chromen-7-yl) acetate
State
State

At room temperature, (4-methyl-2-oxo-coumarin-7-yl) acetate is typically found in a solid state. It retains stability under typical environmental conditions and does not readily sublimate or liquefy.

Melting point (Celsius)
132.00
Melting point (Kelvin)
405.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
216.22g/mol
Molar mass
216.1950g/mol
Density
1.2203g/cm3
Appearence

(4-methyl-2-oxo-coumarin-7-yl) acetate is a solid compound typically appearing as a crystalline substance. It can range in color from yellow to off-white, depending on the purity and specific sample characteristics. As a solid, it exhibits the typical features expected of crystalline structures.

Comment on solubility

Solubility of (4-methyl-2-oxo-chromen-7-yl) acetate

(4-methyl-2-oxo-chromen-7-yl) acetate, with the chemical formula C13H10O4, exhibits interesting solubility characteristics that can be influenced by several factors. Understanding its solubility is crucial for various applications in both research and industry. Here are some important considerations:

  • Solvent Polarity: The solubility of this compound may vary significantly between polar and non-polar solvents. Generally, organic compounds like (4-methyl-2-oxo-chromen-7-yl) acetate tend to be more soluble in non-polar solvents.
  • Temperature Dependency: As with many chemical compounds, solubility can increase with temperature. Heating the solvent may facilitate better dissolution of the acetate.
  • pH Influence: The solubility might also be affected by the pH level of the solvent. Since this compound contains acetyl and carbonyl groups, ionization could alter its solubility in aqueous solutions.
  • Hydrogen Bonding: The presence of functional groups that can engage in hydrogen bonding may enhance solubility in certain polar solvents, allowing for more interaction with the solvent molecules.

In summary, the solubility of (4-methyl-2-oxo-chromen-7-yl) acetate is not just a binary characteristic; it can be influenced by solvent choice, temperature, pH, and molecular interactions. Its behavior in different environments makes it a compound of interest for further exploration in the fields of chemistry and material science.

Interesting facts

Interesting Facts about (4-methyl-2-oxo-chromen-7-yl) acetate

(4-methyl-2-oxo-chromen-7-yl) acetate, often recognized for its unique structure and functional properties, is a fascinating compound within the realm of organic chemistry.

  • Structural Significance: This compound belongs to the class of coumarins, which are well-known for their aromatic characteristics and potential biological activities. The presence of the 4-methyl and 2-oxo groups dramatically influences its chemical reactivity and interactions.
  • Biological Activity: Compounds like (4-methyl-2-oxo-chromen-7-yl) acetate are noteworthy for their potential therapeutic applications. Research has shown that coumarin derivatives exhibit a range of biological activities, including antioxidant, anti-inflammatory, and antimicrobial effects. This makes them of great interest in medicinal chemistry.
  • Synthesis: The synthesis of (4-methyl-2-oxo-chromen-7-yl) acetate can involve a variety of methods, typical for the construction of coumarin structures. These may include the use of simple starting materials and efficient reaction pathways, offering insight into organic synthesis techniques.
  • Nature’s Inspiration: The charm of coumarins, including (4-methyl-2-oxo-chromen-7-yl) acetate, is often drawn from their natural occurrence. They can be found in numerous plants and are responsible for many of the scents and flavors we associate with certain flowers and spices.
  • Cultural Relevance: Beyond their chemical properties, coumarins have historical significance in the fragrance and flavor industry. Their derivatives are often used in perfumery and food industries, contributing to both the aromatic profile and the sensory experience.

In conclusion, (4-methyl-2-oxo-chromen-7-yl) acetate exemplifies the intricate relationship between structure and function in organic chemistry. With its intriguing properties and potential applications, it offers a compelling subject of study for both students and researchers alike.

Synonyms
7-Acetoxy-4-methylcoumarin
4-methylumbelliferyl acetate
2747-05-9
4-Methyl-2-oxo-2H-chromen-7-yl acetate
2H-1-Benzopyran-2-one, 7-(acetyloxy)-4-methyl-
(4-methyl-2-oxochromen-7-yl) acetate
beta-Methylumbelliferyl acetate
7-(Acetyloxy)-4-methyl-2-benzopyrone
Hymecromone Acetate
MFCD00006865
4-methyl-7-acetyloxy coumarin
CHEBI:17763
ZD294D576M
NSC-1059
NSC-31658
NSC-44763
MLS000554751
.beta.-Methylumbelliferyl acetate
7-acetoxy-4-methylchromen-2-one
DTXSID70181895
NSC 1059
Acetic acid 4-methyl-2-oxo-2H-chromen-7-yl ester
EINECS 220-386-6
NSC 31658
NSC 44763
NSC688806
7-(ACETYLOXY)-4-METHYLCOUMARIN
.BETA.-METHYLUMBELLIFERONE ACETATE
SMR000146868
7-HYDROXY-4-METHYLCOUMARIN ACETATE
7-Acetoxy-4-methyl-2H-1-benzopyran-2-one
7-(acetyloxy)-4-methyl-2H-1-benzopyran-2-one
COUMARIN, 7-HYDROXY-4-METHYL-, ACETATE
b-methylumbelliferyl acetate
4-MUA
ACETYL HYMETOCHROME
cid_366
7-Acetoxy-4-methyl coumarin
(4-methyl-2-oxidanylidene-chromen-7-yl) ethanoate
CHEMBL12019
SCHEMBL335474
UNII-ZD294D576M
4-Methyl Umbelliferone Acetate
IFLab1_001442
IFLab2_000119
MEGxp0_001897
4-Methyl-umbelliferone, acetate
b-Methylumbelliferyl acetic acid
4-Methylumbelliferyl acetic acid
BDBM33456
DTXCID10104386
NSC1059
beta-Methylumbelliferyl acetic acid
HMS1416B12
HMS2290M10
ALBB-020396
BCP21289
NSC31658
NSC44763
4-Methylumbelliferyl acetate - 95%
STK395120
AKOS000323400
BETA-METHYLUMBELLIFERONE ACETATE
CCG-214462
NSC-688806
IDI1_019145
(4-methyl-2-oxo-chromen-7-yl) acetate
4-Methyl-2-oxo-2H-chromen-7-ylacetate
NCGC00246518-01
AC-11030
AS-12521
EM166026
NCI60_000142
NCI60_002720
DB-029341
HY-137877
4-Methyl-2-oxo-2H-chromen-7-yl acetate #
A1527
CS-0142508
EU-0039270
NS00049036
C03837
4-Methylumbelliferyl acetate, esterase substrate
AB00448415-08
Hymecromone Acetate; 4-Methylumbelliferyl Acetate
SR-01000443138
acetic acid (2-keto-4-methyl-chromen-7-yl) ester
SR-01000443138-1
Q27102589
acetic acid (4-methyl-2-oxo-1-benzopyran-7-yl) ester
F0415-0023