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

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Identification
Molecular formula
C10H16Br2Cl2
CAS number
Not Available
IUPAC name
6-bromo-3-(bromomethyl)-3,7-dichloro-7-methyl-oct-1-ene
State
State

The compound is usually found in a liquid state at room temperature.

Melting point (Celsius)
-80.00
Melting point (Kelvin)
193.15
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
345.98g/mol
Molar mass
345.9820g/mol
Density
1.5000g/cm3
Appearence

6-bromo-3-(bromomethyl)-3,7-dichloro-7-methyl-oct-1-ene is typically a colorless to pale yellow liquid.

Comment on solubility

Solubility of 6-bromo-3-(bromomethyl)-3,7-dichloro-7-methyl-oct-1-ene (C10H16Br2Cl2)

The solubility of 6-bromo-3-(bromomethyl)-3,7-dichloro-7-methyl-oct-1-ene can be considered with certain factors in mind:

  • Polarity: Given the presence of multiple halogens (Br and Cl) in its structure, this compound exhibits a level of polarity that influences its interaction with solvents.
  • Solvent Compatibility: This compound is likely to have limited solubility in water due to the hydrophobic character of the hydrocarbon chain, making it more soluble in non-polar or slightly polar organic solvents such as:
    • Hexane
    • Chloroform
    • Acetone
  • Temperature Effect: As with many organic compounds, solubility may increase with temperature, allowing for greater dissolution in organic media.

In conclusion, while the solubility of 6-bromo-3-(bromomethyl)-3,7-dichloro-7-methyl-oct-1-ene is expected to be somewhat limited in polar solvents, it has the potential for better solubility in non-polar organic solvents. As with all chemical compounds, it is essential to perform experimental assessments to confirm these solubility predictions.

Interesting facts

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

The compound 6-bromo-3-(bromomethyl)-3,7-dichloro-7-methyl-oct-1-ene, often abbreviated for convenience, is a fascinating member of the halogenated organic compounds. Its complexity presents a variety of interesting chemical properties and applications:

  • Halogenation: This compound features multiple halogens, including bromine and chlorine. Halogenation plays a critical role in altering the reactivity of organic compounds and is widely used in synthesis.
  • Applications in Agriculture: Compounds like this one are often examined for their potential use as pesticides or herbicides, due to their ability to disrupt biochemical pathways in target organisms.
  • Synthetic Utility: The unique structure makes this compound a valuable intermediate in organic synthesis, particularly in the development of more complex molecules.
  • Study of Reaction Mechanisms: The presence of both bromine and chlorine allows chemists to study various reaction mechanisms involving nucleophilic substitution and elimination reactions.
  • Chiral Centers: Although the molecule is symmetrical, exploring its stereochemistry can unveil different isomers, which have distinct physical and chemical properties.

This compound serves as a prime example of how halogenated organic molecules can be tailored for specific applications while showcasing the intricate behavior of organic reactions. As envisioned by chemists, understanding the reactivity and properties of such compounds can lead to advancements in both industrial and pharmaceutical chemistry.

In the words of scientist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." Examining compounds like 6-bromo-3-(bromomethyl)-3,7-dichloro-7-methyl-oct-1-ene contributes to a wealth of knowledge in organic chemistry and beyond.

Synonyms
CHEMBL1986244
NSC659554
NSC-659554
NCI60_021005
6-Bromo-3-bromomethyl-3,7-dichloro-7-methyl-1-octene