Interesting facts
Interesting Facts about 2,5-Dimethylhexa-2,4-diene
2,5-Dimethylhexa-2,4-diene is a fascinating organic compound with several unique attributes that capture the interest of chemists and students alike. Here are some noteworthy facts:
- Structure: This compound features a complex arrangement of double bonds and substituents, contributing to its reactivity and versatility in chemical reactions.
- Isomerism: With multiple double bonds present in its structure, 2,5-dimethylhexa-2,4-diene exhibits geometric isomerism, which means it can exist in different forms that have distinct physical and chemical properties.
- Applications: Compounds with similar structures are often utilized in the synthesis of various organic materials, including pharmaceuticals and polymers, demonstrating the importance of such diene compounds in industrial chemistry.
- Synthesis: Knowledge of synthetic pathways for creating 2,5-dimethylhexa-2,4-diene can be advantageous. It is often produced through the dehydrogenation of saturated hydrocarbons, emphasizing practical applications in organic synthesis.
- Reactivity: The presence of conjugated double bonds makes this compound particularly reactive, allowing it to engage in electrophilic addition reactions that can lead to a variety of new substances in organic chemistry.
- Research Significance: Understanding the properties and behavior of this compound is essential for researchers focused on developing new materials, conducting mechanistic studies, and exploring reaction mechanisms.
As with many organic compounds, the study of 2,5-dimethylhexa-2,4-diene not only enhances our knowledge of chemical structures but also opens up avenues for innovative applications in different fields, from materials science to medicinal chemistry.
If you ask a chemist about this compound, they might say: "Its unique structure and reactivity profile make it a wonderful example of the complexities of organic compounds."
Synonyms
2,5-DIMETHYL-2,4-HEXADIENE
764-13-6
Biisocrotyl
Biisobutenyl
Diisocrotyl
2,5-Dimethylhexa-2,4-diene
2,4-Hexadiene, 2,5-dimethyl-
NSC 10812
EINECS 212-115-5
EE5YRI32X6
AI3-26989
NSC-10812
DTXSID3022116
1,1,4,4-TETRAMETHYLBUTA-1,3-DIENE
2,5Dimethylhexa2,4diene
2,4Hexadiene, 2,5dimethyl
DTXCID102116
inchi=1/c8h14/c1-7(2)5-6-8(3)4/h5-6h,1-4h
C8H14
UNII-EE5YRI32X6
1,1,4,4-Tetramethylbuta-1,3-diene; Biisobutenyl; Biisocrotyl; Diisocrotyl; NSC 10812;
NSC10812
2,4-diene
2,5dimethyl-2,4-hexadiene
2,5-dimethyl-hexa-2,4-diene
CHEBI:88821
(CH3)2C=CHCH=C(CH3)2
MFCD00008904
2,5-Dimethyl-2,4-hexadiene, 96%
AKOS009157108
LS-13467
D0735
NS00037782
A838694
2,5-dimethyl-2,4-hexadiene (stabilized with bht)
Q27160797
F0001-1940
Solubility of 2,5-Dimethylhexa-2,4-diene
2,5-Dimethylhexa-2,4-diene is an organic compound characterized by its unique structure. When discussing its solubility, several factors come into play.
Solubility Characteristics
This compound is known to be:
As stated, "like dissolves like"; thus, understanding the polarity of your solvent is critical when working with 2,5-dimethylhexa-2,4-diene. In laboratory settings, it’s essential to choose appropriate solvents to optimize dissolution.
Key Takeaway
This compound's solubility profile highlights the significance of molecular structure in influencing interactions with solvents, making it a valuable study material for understanding solubility principles in organic chemistry.