Interesting facts
Interesting Facts about 5-Methylhexane-2,3-dione
5-Methylhexane-2,3-dione is a fascinating organic compound that belongs to the family of diketones. It plays a significant role in various chemical reactions and is often studied for its interesting properties and applications. Here are some intriguing facts about this compound:
- Structure and Isomerism: 5-Methylhexane-2,3-dione exhibits notable structural features, including two carbonyl groups (C=O) situated at the 2 and 3 positions of the hexane chain. This positioning leads to the potential for geometric and positional isomerism, making it an essential study subject in organic chemistry.
- Synthesis: The synthesis of this diketone can involve various routes, including the condensation of acetylacetone derivatives. Its preparation often serves as a valuable demonstration of reaction mechanisms in advanced organic chemistry courses.
- Reactivity: As a diketone, 5-methylhexane-2,3-dione participates in numerous reactions, such as aldol condensations and Michael additions. These transformations are fundamental in the synthesis of more complex organic molecules, showcasing the compound's utility in organic synthesis.
- Applications: This compound is studied for its potential applications in areas like pharmaceuticals, agrochemicals, and materials science. The diketone structure is essential in designing molecules with specific properties and functions.
- Biological Significance: While research on the biological activity of 5-methylhexane-2,3-dione is still emerging, compounds with diketone structures often display interesting biological properties, which could lead to novel drug discovery insights.
In conclusion, 5-methylhexane-2,3-dione is not just another diketone; it embodies the intricacies of organic chemistry and highlights the importance of understanding structural and reactivity patterns in chemical compounds. As one delves deeper into its study, the potential for discovering new applications and enhancing existing processes becomes apparent.
Synonyms
5-Methylhexane-2,3-dione
5-Methyl-2,3-hexanedione
13706-86-0
Acetyl isovaleryl
2,3-HEXANEDIONE, 5-METHYL-
Acetylisopentanoyl
Acetyl isopentanoyl
Acetylisovaleryl
2-Methylhexa-4,5-dione
FEMA No. 3190
EINECS 237-241-8
UNII-ZI95KZ32L4
Isobutylmethylglyoxal
BRN 1745751
ZI95KZ32L4
DTXSID7049215
DTXCID3029071
FEMA 3190
4-01-00-03701 (Beilstein Handbook Reference)
METHYL-2,3-HEXANEDIONE, 5-
5-METHYL-2,3-HEXANEDIONE [FHFI]
2-Methyl-4,5-hexanedione
MFCD00059352
Isobutyl methyl diketone
5-methyl-hexane-2,3-dione
SCHEMBL93309
CHEMBL3186524
CHEBI:173493
PQCLJXVUAWLNSV-UHFFFAOYSA-N
Tox21_202802
AKOS022180886
NCGC00260348-01
BS-42681
DA-37135
FM167654
CAS-13706-86-0
M0752
NS00021631
D84272
Q27295570
5-Methyl-2,3-hexanedione 100 microg/mL in Acetonitrile
5-Methyl-2,3-hexanedione; 2-Methylhexa-4,5-dione; 5-methyl-2,3-hexanedione
Solubility of 5-methylhexane-2,3-dione
5-methylhexane-2,3-dione, also known as an intermediate in organic synthesis, exhibits specific solubility characteristics that are essential for its applications in various chemical processes. Understanding its solubility can provide insights into its reactivity, compatibility, and utilization. Here are some key points regarding its solubility:
In summary, while the solubility of 5-methylhexane-2,3-dione is influenced by its molecular structure, it demonstrates a preference for polar environments. This is important for chemists who aim to use this compound in synthetic applications where solvent choice is crucial for successful reactions.