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Allethrin

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Identification
Molecular formula
C19H26O3
CAS number
584-79-2
IUPAC name
(5-allyl-2-furyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate
State
State

At room temperature, allethrin is a dense liquid. It does not readily crystallize and maintains a liquid state under normal atmospheric conditions. This characteristic makes it suitable for use in various spray and liquid dispenser formulations.

Melting point (Celsius)
-78.00
Melting point (Kelvin)
195.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
302.41g/mol
Molar mass
302.4140g/mol
Density
0.8770g/cm3
Appearence

Allethrin appears as a viscous liquid, typically yellow to amber in color. Its appearance can vary depending on its purity and formulation, but it generally presents as a clear to slightly turbid liquid.

Comment on solubility

Solubility of (5-allyl-2-furyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate

Understanding the solubility of a compound like (5-allyl-2-furyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate can be quite intricate due to its complex structure. Here are some key considerations regarding its solubility:

  • Polar vs Nonpolar: The presence of various functional groups (such as furan and allyl) indicates that this compound may exhibit both polar and nonpolar characteristics. This duality can affect its solubility in different solvents.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as ethanol, acetone, or dichloromethane due to its organic nature, but may have limited solubility in aqueous solutions.
  • Temperature Effects: The solubility may increase with temperature, a common trend observed with many organic compounds, making it important in practical applications.
  • Functional Group Interaction: The interaction of polar functionalities with water could lead to certain solubility behavior, potentially making it soluble under specific conditions or pH.

Overall, the solubility behavior of this compound can be summarized as being influenced by multiple factors, which highlights the need for empirical testing to determine its precise solubility in various environments. Thus, understanding its interactions with solvents is crucial for both research and application purposes.

Interesting facts

Interesting Facts about (5-allyl-2-furyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate

(5-allyl-2-furyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate is a remarkable compound with unique structural attributes and potential applications that capture the interest of chemists and students alike. Here are some intriguing insights into this fascinating chemical:

  • Structural Complexity: The compound features a complex structure that integrates a furan ring, a cyclopropane moiety, and multiple substituents, making it a vivid example of organic synthesis creativity. This complexity often leads to unique reactivity and properties.
  • Natural Compounds Connection: The furan ring in its structure links it to a class of compounds found in nature. Furans are known for their occurrence in various essential oils and as intermediates in the synthesis of some natural products.
  • Potential Applications: Given its unique functional groups, this compound could exhibit interesting biological activities, possibly serving as a lead structure for the development of pharmaceuticals or agrochemicals. The cyclopropane moiety is particularly notable for its efficacy in modifying the biological properties of compounds.
  • Versatility: The presence of multiple double bonds suggests a variety of possible reactions, including polymerization or further functionalization, providing ample opportunities for synthetic chemists to explore.

In essence, (5-allyl-2-furyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate stands as a prime example of how intricate chemical structures can open doors to various scientific inquiries. As a student or a researcher, delving into the chemistry of such compounds can yield profound insights into organic chemistry and materials science.

Synonyms
5-Allylfurfuryl chrysanthemate
10597-73-6
Japothrins
2,2-Dimethyl-3-(2-methylpropenyl)cyclopropanecarboxylic acid 5-allylfurfuryl ester
Cyclopropanecarboxylic acid, 2,2-dimethyl-3-(2-methylpropenyl)-, 5-allylfurfuryl ester
DTXSID9057927