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Bromocycloheptane

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Identification
Molecular formula
C7H13Br
CAS number
177-81-7
IUPAC name
bromocycloheptane
State
State

At room temperature, bromocycloheptane exists as a liquid.

Melting point (Celsius)
-39.00
Melting point (Kelvin)
234.15
Boiling point (Celsius)
187.50
Boiling point (Kelvin)
460.65
General information
Molecular weight
177.08g/mol
Molar mass
177.0560g/mol
Density
1.3129g/cm3
Appearence

Bromocycloheptane is a clear to pale yellow liquid. It may also exhibit a faint unpleasant odor, typical of brominated compounds.

Comment on solubility

Solubility of Bromocycloheptane

Bromocycloheptane, with the chemical formula C7H11Br, exhibits interesting solubility characteristics that can be primarily attributed to its molecular structure and the presence of the bromine atom. Here are some key points regarding its solubility:

  • Non-polar Nature: Due to its cycloalkane structure, bromocycloheptane is largely non-polar. This property influences its solubility in solvents.
  • Solvent Compatibility: It tends to dissolve well in non-polar solvents such as hexane or benzene, which can accommodate its hydrophobic characteristics.
  • Poor Solubility in Water: Conversely, bromocycloheptane has poor solubility in polar solvents such as water. This is primarily due to the inability to form significant interactions with water molecules.

In summary, bromocycloheptane's solubility is a reflection of its molecular characteristics, exemplifying the general rule that "like dissolves like." This principle highlights why its solubility is favorable in non-polar environments while being hindered in polar ones.

Interesting facts

Interesting Facts about Bromocycloheptane

Bromocycloheptane is an intriguing compound that falls within the realm of cyclic hydrocarbons, particularly cyclic alkanes. Here are some fascinating aspects associated with this compound:

  • Structure and Stability: Bromocycloheptane features a cycloheptane ring with a bromine atom attached, which adds polar character and influences its reactivity. The strain in the seven-membered ring can lead to interesting chemical behavior when involved in reactions.
  • Reactivity: The presence of the bromine atom makes bromocycloheptane a versatile intermediate in organic synthesis. It can participate in nucleophilic substitution reactions, making it valuable for constructing more complex organic molecules.
  • Applications: Compounds like bromocycloheptane can be utilized in the synthesis of pharmaceuticals and agrochemicals. Their unique structure often leads to compounds with potent biological activity, making them of interest in medicinal chemistry.
  • Related Compounds: Cycloheptane itself is interesting, but the introduction of bromine opens the door to many other derivatives. This can lead to a diverse array of functionalized compounds, each with unique properties.
  • Safety Considerations: As with many brominated compounds, caution is advised when handling bromocycloheptane due to potential toxicity and environmental concerns. Proper safety protocols should always be followed in the lab.

As a result of these characteristics, bromocycloheptane serves as a valuable compound in both academic research and industrial applications, highlighting the complexity and utility of halogenated alicyclic compounds in organic chemistry.

Synonyms
BROMOCYCLOHEPTANE
Cycloheptane, bromo-
EINECS 219-294-9
NSC 9472
DTXSID1062386
DTXCID8036994
219-294-9
loxorfrcpxuorp-uhfffaoysa-n
2404-35-5
Cycloheptyl bromide
bromo-cycloheptane
MFCD00004149
NSC-9472
Cycloheptylbromide
bromocyclo-heptane
NSC9472
2-bromocycloheptane
Cycloheptane,bromo-
Bromocycloheptane, 97%
LC8AX2EKR3
SCHEMBL625207
CHEBI:183290
CAA40435
AKOS009159096
SY043335
DB-046328
CS-0146614
NS00027545
EN300-124124
F53566