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2-Iodooctane

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Identification
Molecular formula
C8H17I
CAS number
4235-95-4
IUPAC name
2-iodooctane
State
State

This compound is in a liquid state at room temperature.

Melting point (Celsius)
-51.00
Melting point (Kelvin)
222.10
Boiling point (Celsius)
216.20
Boiling point (Kelvin)
489.30
General information
Molecular weight
240.13g/mol
Molar mass
240.1250g/mol
Density
1.2097g/cm3
Appearence

2-Iodooctane is a colorless to pale yellow liquid. It may appear slightly oily and has a characteristic odor typical of alkyl iodides.

Comment on solubility

Solubility of 2-iodooctane

2-iodooctane, with the chemical formula C8H17I, exhibits interesting solubility characteristics influenced by its structure. As an alkyl halide, it includes a hydrophobic carbon chain and a polar iodine atom. This dual nature results in the following solubility behavior:

  • Solvent Compatibility: 2-iodooctane is primarily soluble in organic solvents such as hexane and toluene, owing to its non-polar hydrocarbon chain.
  • Water Solubility: It shows low solubility in water due to the hydrophobic character of the long carbon chain, which cannot effectively interact with water molecules.
  • Applications: Its solubility profile makes it useful in organic synthesis and as a reagent, especially in reactions involving lipophilic environments.

This unique balance of hydrophobic and polar properties leads to the understanding that **2-iodooctane will primarily favor non-polar environments**, making it less suited for aqueous solutions. In practical terms, when working with this compound, consider utilizing organic solvents for dissolution or reaction processes.

Interesting facts

Interesting Facts About 2-Iodooctane

2-Iodooctane is an intriguing compound that belongs to the family of alkyl halides, specifically a member of the octane family. It is primarily recognized for its unique properties and applications in various scientific fields.

Key Characteristics and Applications:

  • Structural Importance: This compound features an iodine atom attached to the second carbon of the octane chain, distinguishing it from other octanes and imparting its distinctive chemical behavior.
  • Synthesis: 2-Iodooctane can be synthesized through halogenation reactions, where iodine is introduced to octane under appropriate conditions, highlighting the fascinating world of organic synthesis.
  • Use in Organic Reactions: It serves as a useful reagent in organic chemistry, particularly in nucleophilic substitution reactions, where the iodine atom can be replaced by various nucleophiles.
  • Role in the Pharmaceutical Industry: Compounds like 2-iodooctane often play a role in drug design and development due to their ability to alter the lipophilicity of the compounds they are incorporated into.
  • Hydrophobic Characteristics: Its hydrophobic nature makes it an ideal candidate for studying interactions in lipid membranes and for applications in materials science.

Cultural and Economic Impact:

While perhaps not famous in popular culture, compounds like 2-iodooctane contribute significantly to various industries, making it a noteworthy compound in the realm of chemistry. As research continues to evolve, the potential uses and understanding of 2-iodooctane may expand even further.

"In the world of organic chemistry, each compound tells its own unique story, and 2-iodooctane is no exception." - A budding chemist

The exploration of 2-iodooctane provides an excellent opportunity for students and researchers alike to delve into the complexities of molecular interactions and the significant roles such compounds play in science and technology.

Synonyms
2-IODOOCTANE
Octane, 2-iodo-
sec-Octyl iodide
EINECS 209-172-3
UNII-89710GTW4Y
89710GTW4Y
SEC-OCTYL IODIDE [MI]
DTXSID90870613
2Iodooctane
2Octyl iodide
Octane, 2iodo
DTXCID20217779
209-172-3
(+-)-2-octyl iodide
xflogtufkzcftk-uhfffaoysa-n
557-36-8
2-Octyl iodide
(+/-)-2-OCTYL IODIDE
2-iodo-octane
SCHEMBL6032249
ALBB-036478
STL453657
Octane, 2-iodo-, (.+/-.)-
AKOS009031590
DB-052784
NS00044152
Q27270016