Skip to main content

6-bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyl-oct-1-ene

ADVERTISEMENT
Identification
Molecular formula
C10H12Br2Cl3
CAS number
403616-58-2
IUPAC name
6-bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyl-oct-1-ene
State
State
The compound is a liquid at room temperature.
Melting point (Celsius)
-12.50
Melting point (Kelvin)
260.70
Boiling point (Celsius)
262.30
Boiling point (Kelvin)
535.50
General information
Molecular weight
360.46g/mol
Molar mass
360.4600g/mol
Density
1.5400g/cm3
Appearence

This compound is typically found as a colorless to pale yellow liquid at room temperature. The color can darken upon exposure to light or due to impurities.

Comment on solubility

Solubility of 6-bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyl-oct-1-ene

The solubility characteristics of the compound 6-bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyl-oct-1-ene (C10H12Br2Cl3) can be intriguing due to its complex structure, which includes multiple halogen substituents. Its solubility can vary significantly depending on various factors:

  • Polarity: The presence of bromine and chlorine atoms introduces polar characteristics, suggesting that this compound may be more soluble in polar solvents.
  • Hydrophobic Interactions: With its hydrocarbon backbone, the compound may also exhibit hydrophobic properties, potentially limiting solubility in purely aqueous environments.
  • Temperature Effects: Solubility may increase with temperature, as is common with organic compounds, promoting dissolution in selected organic solvents.
  • Common Solvents: It could be soluble in organic solvents like acetone, ethanol, or dichloromethane but less so in water.

To summarize, the solubility of C10H12Br2Cl3 is highly influenced by its molecular structure and the nature of the solvent used. Understanding these solubility characteristics is crucial in applications where this compound might be utilized, such as in syntheses or in formulations within chemical industries.

Interesting facts

Interesting Facts about 6-bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyl-oct-1-ene

This fascinating compound, known for its intricate structure and multiple halogen substitutions, presents unique characteristics and applications that pique the interest of chemists and researchers alike. Here are some notable aspects:

  • Diverse Halogenation: The presence of both bromine and chlorine atoms makes this compound a prime example of halogenated organic molecules. The addition of these electronegative elements can significantly alter the compound's reactivity and biological activity.
  • Potential Applications: Such compounds often find uses in various fields, including agricultural chemistry as pesticides or herbicides, owing to their ability to disrupt biological processes in target organisms while exhibiting lower toxicity to non-target species.
  • Structural Complexity: The specific arrangement of halogens and the alkenyl group (indicated by the 'oct-1-ene' part of the name) creates opportunities for studying stereochemistry and geometric isomerism, which are crucial in the synthesis of pharmaceuticals.
  • Environmental Considerations: Due to the halogen content, these compounds necessitate careful scrutiny concerning their environmental impact. Many halogenated organic compounds have raised concerns regarding persistence in the environment and potential bioaccumulation.
  • Research Insights: The structural features of this compound can be of interest in material science, particularly in developing innovative materials with unique properties such as enhanced chemical resistance or useful optical characteristics.

In conclusion, 6-bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyl-oct-1-ene serves as a remarkable study subject in both synthetic and applied chemistry. Its diverse applications and implications underscore the importance of understanding the behavior and effects of halogenated compounds in our ever-evolving chemical landscape.

Synonyms
58086-84-3
6-bromo-3-(bromomethyl)-2,3,7-trichloro-7-methyloct-1-ene
NSC662825
HALOMON (RACEMIC)
Neuro_000386
(+)-6-Bromo-3-bromomethyl-2,7-trichloro-7-methyl-1-octene
SCHEMBL6265894
CHEMBL1966017
DTXSID10973670
NSC673501
NSC673502
NSC-662825
NSC-673501
NSC-673502
NCI60_021713
NCI60_026038
NCI60_026039
(-)-6-Bromo-3-bromomethyl-2,7-trichloro-7-methyl-1-octene