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(-)-Menthone

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Identification
Molecular formula
C14H18O4
CAS number
26354-04-3
IUPAC name
7-oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate
State
State

At room temperature, this compound exists as a solid due to its substantial molecular weight and complex structure. Its crystalline form remains stable, and it does not easily transition to a liquid or gaseous state under normal conditions.

Melting point (Celsius)
55.00
Melting point (Kelvin)
328.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
250.27g/mol
Molar mass
250.2740g/mol
Density
1.1725g/cm3
Appearence

7-Oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate typically has a crystalline solid appearance with an often white or off-white color. Its distinct crystalline structure is one notable feature, especially when considering the reflection of light and formation of geometric shapes in crystallography.

Comment on solubility

Solubility of 7-oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate

The solubility of 7-oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate can be influenced by various factors, making it a compound of interest for study. Here are some key points regarding its solubility:

  • Polarity: The presence of functional groups in this compound, such as the carboxylate group, typically enhances solubility in polar solvents like water.
  • Solvent Interaction: It is crucial to consider the solvent used. For instance, this compound may be more soluble in organic solvents like ethanol and acetone than in purely aqueous conditions.
  • Temperature Sensitivity: Like many organic compounds, solubility may increase with temperature, which can affect practical applications in synthesis and reactions.
  • pH Dependence: The ionization state of the carboxylate group will depend on the pH of the solution, which can further influence its solubility characteristics.

In summary, while specific quantitative solubility data for this compound may be limited, understanding its chemical structure and the surrounding environmental factors can provide insights into its behavior in different solvents. As with many organic compounds, practical experimentation remains a fundamental approach to elucidating its solubility properties.

Interesting facts

Interesting Facts about 7-oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate

This compound belongs to a fascinating class of chemicals known as bicyclic compounds, specifically exhibiting a unique bicyclo[4.1.0] structure. Bicyclic compounds are characterized by two fused rings that create distinct architectural arrangements, which play a significant role in the compound's chemical properties and reactivity. Here are some noteworthy aspects:

  • Reaction Potential: The structural arrangement often grants them interesting reaction dynamics, making them valuable in organic synthesis.
  • Pharmaceutical Applications: Compounds with similar structures have been explored for their potential therapeutic uses, particularly in the realm of drug design due to their ability to mimic natural products.
  • Fun Fact: The inclusion of oxygen atoms in the bicyclic framework can affect the compound's properties, enhancing polar characteristics and adding functional versatility.
  • Research Interest: Chemists are continually investigating compounds like this for their potential in the development of new materials or active pharmaceutical ingredients.

Quote: "The beauty of chemistry lies in understanding how small structural changes can lead to significant alterations in properties and functions." This is particularly true for 7-oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate, showcasing the potential for innovation in synthesis.

In conclusion, the intricate structure of this compound serves as a testament to the marvels of organic chemistry, from its synthesis pathways to its possible applications in cutting-edge science.

Synonyms
2386-87-0
3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate
Chissonox 221 monomer
ERL-4221
UT-632
3,4-EPOXYCYCLOHEXYLMETHYL-3,4-EPOXYCYCLOHEXANECARBOXYLATE
HSDB 5873
EINECS 219-207-4
3,4-Epoxycyclohexanecarboxylic acid (3,4-epoxycyclohexylmethyl) ester
(3,4-Epoxycyclohexyl)methyl 3,4-epoxycyclohexylcarboxylate
3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexane carboxylate
BRN 1381750
CCRIS 8882
UVA 1500 MONOMER
7-Oxabicyclo(4.1.0)heptane-3-carboxylic acid, 7-oxabicyclo(4.1.0)hept-3-ylmethyl ester
7-Oxabicyclo[4.1.0]heptane-3-carboxylic acid, 7-oxabicyclo[4.1.0]hept-3-ylmethyl ester
3,4-Epoxycyclohexanemethyl 3,4-epoxycyclohexanecarboxylate
EC 219-207-4
7-Oxabicyclo(4.1.0)hept-3-ylmethyl 7-oxabicyclo(4.1.0)heptane-3-carboxylate
7-Oxabicyclo[4.1.0]hept-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate
37042-87-8
3,4-EPOXYCYCLOHEXANEMETHYL 3,4-EPOXYCYCLOHEXANECARBOXYLATE [HSDB]
7-oxabicyclo[4.1.0]hept-3-ylmethyl7-oxabicyclo[4.1.0]heptane-3-carboxylate
7-oxabicyclo(4.1.0)hept-3-ylmethyl7-oxabicyclo(4.1.0)heptane-3-carboxylate
ERL4221
3,4Epoxycyclohexylmethyl3,4epoxycyclohexanecarboxylate
(3,4Epoxycyclohexyl)methyl 3,4epoxycyclohexylcarboxylate
3,4Epoxycyclohexanemethyl 3,4epoxycyclohexanecarboxylate
3,4Epoxycyclohexylmethyl 3,4epoxycyclohexane carboxylate
3,4-epoxycyclohexylmethyl 3',4'-epoxycyclohexanecarboxylate
3,4Epoxycyclohexanecarboxylic acid (3,4epoxycyclohexylmethyl) ester
7Oxabicyclo(4.1.0)hept3ylmethyl 7oxabicyclo(4.1.0)heptane3carboxylate
7Oxabicyclo(4.1.0)heptane3carboxylic acid, 7oxabicyclo(4.1.0)hept3ylmethyl ester
609-326-3
7-Oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate
DTXSID2027466
S224DEL3P4
3,4-Epoxycyclohexylmethyl 3,4-Epoxycyclohexaneca
DTXCID707466
ECC
CAS-2386-87-0
UT 632
UNII-S224DEL3P4
MFCD00440900
SCHEMBL24975
CHEMBL2143072
BCP32770
Ctcloaliphatic epoxy resin UP-632
Tox21_202388
Tox21_303312
UP-632
AKOS015915254
CS-W012617
NCGC00164163-01
NCGC00164163-02
NCGC00256981-01
NCGC00259937-01
AS-17792
FE160694
DB-028268
NS00011515
F16450
Q19694494
3,4-?Epoxycyclohexylmethyl 3,4-?epoxycyclohexanecarboxylate
3,4-epoxycyclohexylmethyl (3,4-epoxy)cyclohexanecarboxylate
3,4-epoxycyclohexylmethyl-3',4'-epoxycyclohexanecarboxylate
3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate
7-OXABICYCLO(4.1.0)HEPT-3-YLMETHYL 7- OXABICYCLO(4.1.0)HEPTANE-3-CARBOXYLATE
7-Oxabicyclo[4.1.0]hept-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate #
7-OXABICYCLO[4.1.0]HEPTANE-3-CARBOXYLIC ACID,7-OXABICYCLO[4.1.0]HEPT-3-YLMETHYL ESTER
Chissonox 221 monomer;7-Oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate