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Methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate

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Identification
Molecular formula
C16H28Cl2O2
CAS number
67634-12-2
IUPAC name
methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate
State
State

At room temperature, methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate is a liquid, aligning with many organic esters of similar molecular weights.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
290.50
Boiling point (Kelvin)
563.70
General information
Molecular weight
343.28g/mol
Molar mass
343.2800g/mol
Density
1.0568g/cm3
Appearence

Methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate is typically a liquid at room temperature.

Comment on solubility

Solubility of Methyl 7,11-Dichloro-3,7,11-trimethyl-dodec-2-enoate

Methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate presents a unique profile regarding its solubility due to its complex structure. This compound, containing both alkyl and halogen substituents, exhibits varying degrees of solubility in different solvents.

Key Points on Solubility:

  • Polar Solvents: Due to the presence of the ester functional group, methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate shows some solubility in polar solvents such as alcohols and acetone.
  • Non-polar Solvents: The long hydrocarbon chain and the chloro groups contribute to increased solubility in non-polar solvents like hexane and toluene.
  • Pest Management Implications: Its solubility characteristics can impact its efficacy in applications such as pesticides and herbicides. Solubility influences the distribution and bioavailability of the compound in various environments.

In summary, the solubility of methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate can be summarized as a balance between its polar and non-polar interactions. Understanding this solubility behavior is crucial for applications in both research and industry.

Interesting facts

Interesting Facts about Methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate

Methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate is a fascinating compound that falls into the category of esters, specifically derived from fatty acids. Here are some noteworthy points about this unique compound:

  • Antimicrobial Properties: Compounds of this nature often exhibit antimicrobial activity, which has led to research on their potential use in developing natural pesticides and fungicides.
  • Applications in Synthesis: This compound can serve as an intermediate in organic synthesis, providing a pathway to create more complex molecules that are useful in pharmaceuticals and other fine chemicals.
  • Chlorinated Variants: The presence of chlorine atoms in the structure is particularly interesting, as chlorinated compounds are known for their stability and ability to resist degradation, making them important in various industrial applications.
  • Flavor and Fragrance Industry: Similar esters often possess fruity or floral odors, making them valuable in the flavor and fragrance industry where they are used to create pleasing scents in consumer products.
  • Environmental Concerns: The use of chlorinated compounds raises discussions around environmental impact, particularly with regards to their persistence and bioaccumulation in ecosystems.

The study of methyl 7,11-dichloro-3,7,11-trimethyl-dodec-2-enoate demonstrates the intersection of organic chemistry and environmental science, emphasizing how the structural features of a compound can influence its behavior and applications. As scientists and researchers delve deeper, compounds like this continue to reveal new potential while also presenting challenges that require innovative solutions.

In the words of renowned chemist Linus Pauling, "The science of chemistry is the foundation of the planet's life." Understanding compounds like this one contributes significantly to our knowledge and application of chemistry in real-world scenarios.

Synonyms
methyl-3,7,11-trimethyl-7,11-dichloro-2-dodecenoate
10485-39-9
2-DODECENOIC ACID, 7,11-DICHLORO-3,7,11-TRIMETHYL-, METHYL ESTER
DTXSID301171162