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2,3-dimethylpent-1-ene

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Identification
Molecular formula
C7H14
CAS number
563-79-1
IUPAC name
2,3-dimethylpent-1-ene
State
State
At room temperature, 2,3-dimethylpent-1-ene is a liquid.
Melting point (Celsius)
-117.00
Melting point (Kelvin)
156.15
Boiling point (Celsius)
92.00
Boiling point (Kelvin)
365.15
General information
Molecular weight
98.19g/mol
Molar mass
98.1890g/mol
Density
0.7020g/cm3
Appearence
2,3-Dimethylpent-1-ene is a colorless liquid under standard conditions. It may have a slight, characteristic hydrocarbon odor.
Comment on solubility

Solubility of 2,3-Dimethylpent-1-ene

When it comes to the solubility of 2,3-dimethylpent-1-ene (C8H16), it is essential to understand its hydrocarbon nature. This compound is classified as an alkene, specifically a branched alkene, which plays a significant role in its solubility characteristics.

Here are some key aspects of its solubility:

  • Nonpolar Solvent Compatibility: 2,3-dimethylpent-1-ene is expected to be soluble in nonpolar solvents due to its nonpolar molecular structure.
  • Limited Water Solubility: As a hydrocarbon compound, it has very low solubility in water, which is typically a characteristic of nonpolar substances.
  • Typical Aliphatic Behavior: Being an alkene, it might exhibit some degree of solubility in organic solvents, which prefer compounds like itself.

In summary, while 2,3-dimethylpent-1-ene is likely to dissolve well in nonpolar organic solvents, its interaction with water is minimal due to its nonpolar nature. This trend is typical for most alkenes, making them largely hydrophobic.

Interesting facts

Interesting Facts About 2,3-Dimethylpent-1-ene

2,3-Dimethylpent-1-ene is an intriguing compound that belongs to the family of alkenes, characterized by a carbon-carbon double bond in its structure. Here are some fascinating insights into this compound:

  • Structure and Isomerism: The molecular structure of 2,3-dimethylpent-1-ene reveals multiple points of interest. It has two methyl groups attached to the second and third carbons of a five-carbon chain. This structure exhibits geometric isomerism, where the arrangement of substituents around the double bond can lead to different isomers with varying properties.
  • Reactivity: As an alkene, 2,3-dimethylpent-1-ene is known for its reactivity in various chemical reactions, such as addition reactions. The double bond allows it to undergo hydrogenation, halogenation, and polymerization, making it a valuable compound in organic synthesis.
  • Importance in Industry: Compounds similar to 2,3-dimethylpent-1-ene play a significant role in the petrochemical industry. They serve as intermediates in the production of various chemicals and plastics, highlighting the compound's importance in material science and chemical engineering.
  • Occurrence: Interestingly, alkenes like 2,3-dimethylpent-1-ene can also be found naturally in some chemical processes, as they may be generated in small amounts from biomass or during oil refining processes.
  • Historical Perspective: The study of alkenes began in the early 19th century, making 2,3-dimethylpent-1-ene a part of a rich legacy in organic chemistry. Its synthesis and reactions have contributed to essential developments in the field.

In conclusion, 2,3-dimethylpent-1-ene may appear simple, but its fascinating structural features, reactivity, and industrial relevance make it a compound worthy of exploration and study in the world of chemistry. As an alkenes compound, it plays a vital role in the broader context of organic compounds that shape our daily lives.

Synonyms
2,3-DIMETHYL-1-PENTENE
3404-72-6
2,3-Dimethylpent-1-ene
EINECS 222-285-2
DTXSID10863168
NSC 74134
DTXCID90811829
222-285-2
1-Pentene, 2,3-dimethyl-
NSC74134
MFCD00027075
2,3-dimethyl-pent-1-ene
NSC-74134
AKOS009157235
D1248
NS00048105
2,3-Dimethyl-1-pentene, >=97.0% (GC)
T70795