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6-Bromohexan-2-one

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Identification
Molecular formula
C6H11BrO
CAS number
10226-52-3
IUPAC name
6-bromohexan-2-one
State
State

At room temperature, 6-Bromohexan-2-one is in a liquid state.

Melting point (Celsius)
-36.00
Melting point (Kelvin)
237.15
Boiling point (Celsius)
216.00
Boiling point (Kelvin)
489.15
General information
Molecular weight
179.06g/mol
Molar mass
179.0560g/mol
Density
1.2718g/cm3
Appearence

6-Bromohexan-2-one typically appears as a colorless to light yellow liquid. The liquid is clear and can have a faint odor.

Comment on solubility

Solubility of 6-bromohexan-2-one

6-bromohexan-2-one, with the chemical formula C6H11BrO, exhibits fascinating solubility characteristics that are influenced by its molecular structure. As a halogenated ketone, the compound displays varying solubility in different solvents.

Here are some key points regarding the solubility of 6-bromohexan-2-one:

  • Polar Solvents: 6-bromohexan-2-one is likely to have higher solubility in polar solvents such as water due to its potential for hydrogen bonding, although the presence of the bromine atom can decrease this solubility compared to non-halogenated analogs.
  • Non-Polar Solvents: It tends to dissolve more readily in non-polar solvents like hexane or dichloromethane, which can stabilize the hydrophobic (non-polar) parts of its structure.
  • Effect of Temperature: Like many organic compounds, solubility can change with temperature; generally, an increase in temperature enhances solubility.

Overall, while 6-bromohexan-2-one has a degree of polar character, it is primarily characterized by its solubility in non-polar environments. This distinctive behavior emphasizes the importance of understanding the compound's functional groups and molecular interactions in predicting its solubility profile.

Interesting facts

Interesting Facts about 6-Bromohexan-2-one

6-Bromohexan-2-one is a fascinating compound in the realm of organic chemistry. This molecule plays a significant role in various synthetic pathways due to its unique structural attributes and reactivity.

Key Features of 6-Bromohexan-2-one:

  • Halogenation: The presence of the bromine atom in the molecular structure makes this compound a valuable intermediate in organic synthesis. Halogenated compounds, like 6-bromohexan-2-one, are commonly utilized in reactions such as nucleophilic substitutions.
  • Ketone Functional Group: Being a ketone, it possesses a carbonyl group (C=O) which is known to exhibit important chemical properties. Ketones generally participate in nucleophilic addition reactions, making them crucial in synthesizing more complex molecules.
  • Complexity Enhanced: This compound can be used to generate a range of different derivatives. By modifying the side chains or further substituting functional groups, chemists can create a diverse array of compounds, showing the compound’s versatility.

The compound finds applications in various fields, including:

  • Pharmaceuticals: It's often used in the synthesis of important pharmaceutical substances.
  • Agricultural Chemicals: This compound serves as a precursor for certain agrochemicals, demonstrating its importance in agricultural applications.
  • Material Science: Compounds like 6-bromohexan-2-one can be involved in developing new materials with unique properties.

As a testament to its utility, many researchers regard 6-bromohexan-2-one as a building block in synthetic chemistry, often demonstrating that even simple structures can lead to complex and useful products in the laboratory. As stated by chemists: "In the world of organic chemistry, the simplest compounds can yield the most complex outcomes."

Overall, 6-bromohexan-2-one exemplifies the intricate dance of molecular structure and reactivity that is central to organic chemistry.

Synonyms
6-Bromohexan-2-one
10226-29-6
6-BROMO-2-HEXANONE
2-Hexanone, 6-bromo-
EINECS 233-544-4
DTXSID90144846
DTXCID6067337
233-544-4
1-Bromo-5-hexanone
6-bromo-hexan-2-one
5-Oxohexyl Bromide
6-Brom-2-hexanon
MFCD00044891
SCHEMBL1166877
AKOS006274320
DS-16802
SY019728
CS-0155060
NS00023131
EN300-119820
O11558