Interesting facts
Interesting Facts about 1-Iodooctane
1-Iodooctane, a fascinating organic compound, is classified as an alkyl halide due to the presence of a halogen atom, iodine, bonded to a hydrocarbon chain. This compound is notably utilized in various chemical syntheses and applications, which makes it an attractive subject of study in organic chemistry. Here are some intriguing aspects about 1-iodooctane:
- Structure: 1-Iodooctane features a straight-chain structure with an iodine atom attached to the first carbon of an octane chain, making it a primary alkyl iodide. Its structure plays a significant role in its reactivity and interactions with other chemical species.
- Reactivity: As a halogenated compound, 1-iodooctane is known for its reactivity in nucleophilic substitution reactions. This means that it can easily participate in chemical reactions where nucleophiles attack the carbon atom bonded to iodine, leading to the formation of new compounds.
- Synthesis: There are various methods to synthesize 1-iodooctane, including the reaction of octanol with iodine or the reaction of sodium iodide with 1-bromooctane. This versatility in synthesis makes it accessible for laboratory use.
- Applications: 1-Iodooctane serves as an important building block for the manufacture of surfactants, lubricants, and pharmaceuticals. Its utility in organic synthesis also highlights its importance in the field of medicinal chemistry.
- Environmental Impact: As with many organoiodine compounds, the environmental impact of 1-iodooctane is an area of concern. Studying its behavior in ecological systems can provide insights into its persistence and effects on wildlife.
In summary, 1-iodooctane stands out not only for its chemical significance but also for its versatility in various applications. The study of such compounds is vital for advancing our understanding of organic chemistry and developing new materials and pharmaceutical agents.
Synonyms
1-IODOOCTANE
Octane, 1-iodo-
EINECS 211-084-5
BRN 1697479
DTXSID4060868
UWLHSHAHTBJTBA-UHFFFAOYSA-
nOctyl iodide
1Jodoktan
1nOctyl iodide
1Octyl iodide
Octane, 1iodo
DTXCID3043570
211-084-5
4-01-00-00425 (beilstein handbook reference)
inchi=1/c8h17i/c1-2-3-4-5-6-7-8-9/h2-8h2,1h3
uwlhshahtbjtba-uhfffaoysa-n
629-27-6
n-Octyl iodide
Octyl iodide
1-Octyl iodide
1-n-Octyl iodide
1-Jodoktan
1-iodo-octane
1-Jodoktan [Czech]
iodoctane
iodooctane
n-octyliodide
C8H17I
1-iodoctane
1-iodo-n-octane
1-Iodo-n-octane; 1-Octyl Iodide; 1-n-Octyl Iodide; Octyl Iodide; n-Octyl Iodide
MFCD00001105
1-Iodooctane, 98%
KYU7KY3TKH
SCHEMBL84103
1-Iodooctane stabilized with Cu
PDA23208
BBL027322
STK802040
AKOS009031583
1-Iodooctane, purum, >=97.0% (GC)
AS-56382
1-Iodooctane (stabilized with Copper chip)
CS-0188391
I0321
NS00035221
EN300-19406
W18672
Q57905056
F0001-1702
Solubility of 1-Iodooctane
1-Iodooctane, with the chemical formula C8H17I, exhibits some fascinating characteristics regarding its solubility behavior.
As a member of the alkyl halides, 1-iodooctane is primarily composed of a long hydrophobic hydrocarbon chain, which influences its solubility in various solvents:
In summary, 1-iodooctane's limited solubility in water and greater compatibility with organic solvents showcase the traditional solubility rule of "like dissolves like." This property is crucial for applications in organic synthesis and extraction processes.