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2-Bromoheptane

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Identification
Molecular formula
C7H15Br
CAS number
17663-25-5
IUPAC name
2-bromoheptane
State
State

At room temperature, 2-Bromoheptane is a liquid.

Melting point (Celsius)
-93.00
Melting point (Kelvin)
180.15
Boiling point (Celsius)
182.50
Boiling point (Kelvin)
455.65
General information
Molecular weight
179.08g/mol
Molar mass
179.0790g/mol
Density
1.1270g/cm3
Appearence

2-Bromoheptane is a colorless liquid. It may appear slightly yellowish if impure or older. The compound is typically clear and exhibits a characteristic halogenated organic odor.

Comment on solubility

Solubility of 2-bromoheptane

2-bromoheptane, with the chemical formula C7H15Br, exhibits interesting solubility characteristics due to its molecular structure. This compound is classified as a halogenated hydrocarbon, which can influence how it interacts with solvents.

Key Solubility Characteristics:

  • Polarity: 2-bromoheptane possesses a polar bromine atom attached to a relatively nonpolar hydrocarbon chain. This leads to moderate solubility in polar solvents.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as ether and chloroform, while showing limited solubility in water due to the hydrophobic nature of the heptane chain.
  • Temperature Dependency: Like many organic compounds, solubility can increase with temperature; thus, heating the solvent may enhance the solubility of 2-bromoheptane.

In summary, understanding the solubility of 2-bromoheptane is essential for its applications in synthesis and chemical reactions. As a rule of thumb, if you're considering a solvent for 2-bromoheptane, lean towards nonpolar or weakly polar options to ensure optimal solubility.

Interesting facts

Interesting Facts About 2-Bromoheptane

2-Bromoheptane is an organobromine compound that falls under the category of haloalkanes. Here are some intriguing aspects of this compound that highlight its significance in chemistry:

  • Structural Insights: 2-Bromoheptane features a seven-carbon chain (heptane) with a bromine atom attached to the second carbon. This placement of bromine impacts its reactivity and physical properties.
  • Reactiveness: The presence of the bromine atom allows 2-bromoheptane to participate in various nucleophilic substitution reactions. This is key in organic synthesis, where scientists can transform it into a diverse range of compounds.
  • Synthesis: This compound can be synthesized through the free radical bromination of heptane, allowing students to experiment with halogenation reactions and develop practical laboratory skills.
  • Applications: 2-Bromoheptane can serve as an important intermediate in synthesizing more complex organic molecules, making it valuable in drug development and the study of biological activity.
  • Regioselectivity: The regioselectivity of reactions involving 2-bromoheptane often leads to intriguing results, making it a fascinating compound for both students and seasoned chemists alike.

In summary, 2-bromoheptane showcases the rich interplay of structure and reactivity in organic chemistry. As an example of a simple yet versatile molecule, it serves as an excellent educational tool for understanding the principles of halogenated compounds and their utility in synthetic chemistry.

Synonyms
2-BROMOHEPTANE
Heptane, 2-bromo-
DTXSID40870921
EINECS 217-824-3
NSC 11768
DTXCID00818602
217-824-3
hlauceofcoxknf-uhfffaoysa-n
1974-04-5
2-Heptyl bromide
6-bromoheptane
2-bromanylheptane
NSC11768
MFCD00000164
1-Methylhexyl bromide
(1-methyl)hexylbromide
(1-methyl) hexylbromide
SCHEMBL1896962
2-Bromoheptane, technical grade
NSC-11768
AKOS009157870
DB-044953
NS00045381
A813910