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Ascaridole

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Identification
Molecular formula
C10H16O2
CAS number
119-61-9
IUPAC name
1-isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene
State
State

At room temperature, Ascaridole is typically found in a liquid state.

Melting point (Celsius)
-12.90
Melting point (Kelvin)
260.25
Boiling point (Celsius)
190.50
Boiling point (Kelvin)
463.65
General information
Molecular weight
168.23g/mol
Molar mass
168.2340g/mol
Density
1.0770g/cm3
Appearence

Ascaridole appears as a colorless liquid with a distinctive odor. It may also be found in a pale yellow form under specific conditions.

Comment on solubility

Solubility of 1-isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene

The solubility of 1-isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene can be characterized by a range of factors that affect its interaction with various solvents.

Key Factors Influencing Solubility:

  • Molecular Structure: The presence of dioxabicyclo functionality in the compound contributes to its relatively unique solubility profile.
  • Polarity: The overall polarity of the molecule can dictate its solubility in polar versus nonpolar solvents.
  • Hydrogen Bonding: Possible hydrogen bonding interactions may enhance solubility in polar solvents like water.
  • Dispersion Forces: Conversely, the nonpolar regions may show greater solubility in organic solvents.

In practical observations, this compound is generally soluble in organic solvents, such as:

  1. Ethyl acetate
  2. Acetone
  3. Toluene

However, it may exhibit limited solubility in water due to its molecular architecture. The phrasing often used in solubility discussions is that substances are more soluble in solvents of similar polarity, succinctly summarized as "like dissolves like". Thus, for optimal solubility, pairing this compound with other organic solvents is recommended.

Interesting facts

Interesting Facts About 1-Isopropyl-4-Methyl-2,3-Dioxabicyclo[2.2.2]oct-5-ene

1-Isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene is an intriguing compound known for its unique structure and potential applications. Here are some noteworthy aspects that make this compound fascinating:

  • Structural Complexity: The bicyclic framework of this compound, with two fused ring systems, is a prime example of how organic chemistry often combines complexity and function.
  • Potential Applications: Compounds like this often find their use in organic synthesis and can serve as intermediates in the creation of more complex molecules, potentially leading to innovative pharmaceuticals or agrochemicals.
  • Isopropyl and Methyl Groups: The presence of isopropyl and methyl groups in its structure can influence its reactivity, stability, and solubility, making it a subject of interest for chemists focusing on structure-activity relationships.
  • Environmental Considerations: As with many synthetic compounds, understanding their environmental impact and degradation pathways is essential, particularly in the context of sustainability in chemical production.
  • Synergistic Effects: The arrangement of the dioxabicyclo moiety in this compound can create synergistic effects that may enhance or reduce reactivity, making it a great subject for further study in reaction mechanisms.

As a chemist, one might ponder the implications of this compound not just in terms of its structure, but also in its potential future roles in organic synthesis and material science. Studying compounds like 1-isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene reveals how intricate designs in molecular architecture can lead to significant advancements in various fields.

Synonyms
ASCARIDOLE
512-85-6
Ascaridol
1,4-Peroxido-p-menthene-2
1,4-Peroxy-p-menth-2-ene
1,4-Epidioxy-p-menth-2-ene
Ascaricum
Ascarisin
Askaridol
2,3-Dioxabicyclo[2.2.2]oct-5-ene, 1-methyl-4-(1-methylethyl)-
NSC 406266
CHEBI:2866
1-Methyl-4-(1-methylethyl)-2,3-dioxabicyclo(2.2.2)oct-5-ene
2,3-Dioxabicyclo(2.2.2)oct-5-ene, 1-isopropyl-4-methyl-
2,3-Dioxabicyclo(2.2.2)oct-5-ene, 1-methyl-4-(1-methylethyl)-
NSC-406266
NSC-406924
p-Menth-2-ene, 1,4-epidioxy-
1-methyl-4-(1-methylethyl)-2,3-dioxabicyclo[2.2.2]oct-5-ene
EINECS 208-147-4
UNII-1718D0GEVJ
AI3-11049
1-Isopropyl-4-methyl-2,3-Dioxabicyclo(2.2.2)oct-5-ene
1-Isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene
4-methyl-1-(propan-2-yl)-2,3-dioxabicyclo[2.2.2]oct-5-ene
4-methyl-1-(propan-2-yl)-2,3-dioxabicyclo(2.2.2)oct-5-ene
208-147-4
(+-)-ascaridole
ascaridole (mart.)
ascaridole, (+-)-
Ascaridiol
cis-Ascaridole
1-methyl-4-propan-2-yl-2,3-dioxabicyclo[2.2.2]oct-5-ene
1,4-Epidioxy-2-p-menthene
2, 1-isopropyl-4-methyl-
p-Menth-2-ene,4-epidioxy-
2, 1-methyl-4-(1-methylethyl)-
WLN: T66 A B AO BO DUTJ CY F
Ascaridole (organic peroxide) [Forbidden]
Uncinacina
Ascapurin
1-methyl-4-(propan-2-yl)-2,3-dioxabicyclo[2.2.2]oct-5-ene
Kebal II
SCHEMBL156673
1, 4-Peroxy-p-menth-2-ene
CHEMBL467614
1, 4-Epidioxy-p-menth-2-ene
NSC406266
NSC406924
AKOS004910035
FA179595
TS-08412
HY-118494
CS-0066135
NS00010548
C09836
G86204
Q419442
1-isopropyl-4-methyl-7-oxabicyclo[2.2.1]hept-2-ene
1-Isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene #
1-Methyl-4-(1-methylethyl)-2,3-dioxabicyclo[2.2.2]oct-5-ene, 9CI