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[1-[6-(1,1-dimethylallyl)-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]-1-methyl-ethyl] acetate

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Identification
Molecular formula
C23H26O5
CAS number
20307-84-0
IUPAC name
[1-[6-(1,1-dimethylallyl)-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]-1-methyl-ethyl] acetate
State
State

This compound is typically a solid at room temperature, often presenting as a crystalline material.

Melting point (Celsius)
122.30
Melting point (Kelvin)
395.50
Boiling point (Celsius)
250.50
Boiling point (Kelvin)
523.70
General information
Molecular weight
382.43g/mol
Molar mass
382.4280g/mol
Density
1.2000g/cm3
Appearence

The compound typically appears as a pale yellow crystalline solid, depending on its purity and form.

Comment on solubility

Solubility of 1-[6-(1,1-dimethylallyl)-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]-1-methyl-ethyl acetate

The solubility of 1-[6-(1,1-dimethylallyl)-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]-1-methyl-ethyl acetate can be influenced by several factors due to its complex structure. Here are some key points to consider:

  • Polarity: The presence of both hydrophilic acetate groups and hydrophobic hydrocarbon chains impacts the solubility balance in different solvents.
  • Solvent Compatibility: This compound is expected to exhibit better solubility in organic solvents such as:
    • Ethyl acetate
    • Dichloromethane
    • Acetone
  • Temperature Dependence: As with many organic compounds, solubility can increase with temperature, enhancing solvation.
  • Concentration Effects: At higher concentrations, solubility may be reduced due to potential interactions like aggregation.

In summary, while precise solubility data may be scarce due to the compound's unique structure, understanding the interactions of its components gives insight into its behavior in various solvent systems. As a general guideline, solutes tend to dissolve best in solvents that have a similar polarity — a principle worth keeping in mind as you experiment with this compound.

Interesting facts

Interesting Facts about 1-[6-(1,1-Dimethylallyl)-7-Oxo-2,3-Dihydrofuro[3,2-g]Chromen-2-Yl]-1-Methyl-Ethyl Acetate

This fascinating compound belongs to a class of chemicals known as chromenes, which are recognized for their diverse biological activities. Here's what makes this acetylated chromene particularly intriguing:

  • Natural Occurrence: Compounds similar to this one are often found in various plants, contributing to their flavors, fragrances, and protective properties against pests and diseases. This highlights the compound's ecological significance.
  • Biological Activities: Studies have shown that chromenes possess a variety of pharmacological properties, including antioxidant, anti-inflammatory, and potential anti-cancer activities. This opens avenues for research into their potential therapeutic benefits.
  • Structure-Activity Relationships: The unique arrangement of functional groups in this compound can be linked to its biological efficacy. Understanding these relationships is crucial in medicinal chemistry for designing new drugs.
  • Synthetic Pathways: Synthesis of complex organic molecules like this compound is often a multi-step process. Chemists employ various techniques, including reaction optimization and catalytic methods, to enhance yield and efficiency.

Overall, this compound not only serves as a model for studying the properties of chromenes but also represents the continuous interplay between nature and chemistry. As research expands, compounds like this one hold the potential to shape future developments in pharmaceutical sciences.

Synonyms
Rutamarin
14882-94-1
2-[6-(2-methylbut-3-en-2-yl)-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yl acetate
DTXSID501030750
2-(6-(2-methylbut-3-en-2-yl)-7-oxo-2,3-dihydrofuro(3,2-g)chromen-2-yl)propan-2-yl acetate
DTXCID101445600
2-(1-acetyloxy)-(1-methylethyl)-6-(1,1-dimethyl-2-propenyl)-2,3-dihydro-7H-furo(3,2-g)(1)benzopyran-7-one
Chalepin acetate
(+/-)-Rutamarin
Rutamarin, (+/-)-
2UKD4797WG
7H-Furo(3,2-g)(1)benzopyran-7-one, 2-(1-(acetyloxy)-1-methylethyl)-6-(1,1-dimethyl-2-propenyl)-2,3-dihydro-
NSC263654
1092383-76-0
7H-Furo(3,2-g)(1)benzopyran-7-one, 2,3-dihydro-6-(1,1-dimethylallyl)-2-(1-hydroxy-1-methylethyl)-, acetate
[1-[6-(1,1-dimethylallyl)-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]-1-methyl-ethyl] acetate
2-(1-(Acetyloxy)-1-methylethyl)-6-(1,1-dimethyl-2-propen-1-yl)-2,3-dihydro-7H-furo(3,2-g)(1)benzopyran-7-one
2-(6-(2-methylbut-3-en-2-yl)-7-oxo-2,3-dihydro-7H-furo[3,2-g]chromen-2-yl)propan-2-yl acetate
7H-Furo(3,2-g)(1)benzopyran-7-one, 2-(1-(acetyloxy)-1-methylethyl)-6-(1,1-dimethyl-2-propen-1-yl)-2,3-dihydro-
CCRIS 4345
NSC 263654
BRN 1400300
NSC-263654
UNII-2UKD4797WG
2-(1-(Acetyloxy)-1-methylethyl)-6-(1,1-dimethyl-2-propenyl)-2,3-dihydro-7H-furo(3,2-g)(1)benzopyran-7-one
5-19-06-00053 (Beilstein Handbook Reference)
SCHEMBL3414299
CHEMBL1917738
AWMHMGFGCLBSAY-UHFFFAOYSA-N
CHEBI:196315
NAA16405
PAA88294
2-(1-Acetyloxy-1-methylethyl)-6-(1,1-dimethyl-2-propenyl)-2,3-dihydro-7H-furo(3,2-g)(1)benzopyran-7-one
NS00101187
Q27255620
1-[6-(1,1-Dimethylprop-2-en-1-yl)-7-oxo-2,3-dihydro-7H-furo[3,2-g]chromen-2-yl]-1-methylethyl acetate
2-[6-(2-methylbut-3-en-2-yl)-7-oxo-2,3-dihydrouro[3,2-g]chromen-2-yl]propan-2-yl acetate
2-[6-(2-METHYLBUT-3-EN-2-YL)-7-OXO-2H,3H,7H-FURO[3,2-G]CHROMEN-2-YL]PROPAN-2-YL ACETATE