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

Identification

Molecular formula

C₁₀H₁₄Br₂Cl₃

CAS number

IUPAC name

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

State

The compound is typically found as a liquid at room temperature. It can be manipulated and stored under standard laboratory conditions with care due to its halogenated nature.

Melting point (Celsius)

-15.00

Melting point (Kelvin)

258.15

Boiling point (Celsius)

235.00

Boiling point (Kelvin)

508.15

General information

Molecular weight

424.84g/mol

Molar mass

424.8380g/mol

Density

1.6500g/cm³

Appearence

The compound is typically a colorless to pale yellow liquid. It may have a faint characteristic odor. In pure form, it might be less commonly encountered due to its specific chemical synthesis and usage profile.

Comment on solubility

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

The solubility of 7-bromo-3-(bromomethyl)-2,3,6-trichloro-7-methyl-oct-1-ene (C₁₀H₁₄Br₂Cl₃) is an intriguing aspect due to its complex halogenated structure. Generally, the solubility of halogenated compounds can be influenced by several factors:

Polarity: The presence of multiple bromine and chlorine atoms increases the compound's polarity, which can alter its interaction with solvents.
Hydrophobic Characteristics: The long hydrocarbon chain contributes to a hydrophobic nature, often making the compound less soluble in water but potentially more soluble in organic solvents.
Temperature Dependency: Like many organic compounds, solubility can increase with temperature, affecting its dissolution in various solvents.

In general, you can expect such a compound to exhibit:

A low solubility in water due to its hydrophobic characteristics.
Higher solubility in organic solvents, such as acetone or hexane, due to its non-polar aspects.
Potential challenges in solubility testing because of its complex structure and multiple substituents.

In summary, while the compound is likely to be sparingly soluble in polar solvents, it may readily dissolve in non-polar organic solvents, highlighting the importance of solvent choice in any dissolution experiments.

Interesting facts

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

7-bromo-3-(bromomethyl)-2,3,6-trichloro-7-methyl-oct-1-ene is a fascinating organic compound notable for its complex structure and diverse applications. Here are some intriguing points about this compound:

Complex Halogenation: This compound features multiple halogen substituents - three chlorine atoms and two bromine atoms. This level of halogenation gives it unique reactivity and physical properties.
Rearward Design: The oct-1-ene moiety in its name indicates that it has an alkene functional group, which is crucial for its chemical reactivity, such as undergoing additions and polymerizations.
Potential Applications: Compounds like this one are often used in synthetic organic chemistry. They can serve as intermediates in the production of agrochemicals, pharmaceuticals, or advanced materials.
Biological Activity: Many brominated and chlorinated compounds exhibit notable biological activities, which could indicate that this compound may also have interesting effects in biochemical contexts.
Synthetic Challenge: The multi-layered halogenation process that leads to such a complex structure presents unique challenges in terms of synthesis, making it an interesting subject for chemists to explore innovative synthetic pathways.

As scientists continue to delve into the properties and applications of compounds like 7-bromo-3-(bromomethyl)-2,3,6-trichloro-7-methyl-oct-1-ene, it is clear that the field of organic chemistry continually expands our understanding of chemical diversity and functionality. The potential for discovering new applications and enhancing existing methodologies through such compounds can lead to breakthroughs in various industries.