Interesting facts
Interesting Facts about 2,6-Dimethylhepta-2,5-dien-4-one
2,6-Dimethylhepta-2,5-dien-4-one is a fascinating organic compound that belongs to the class of ketones and possesses unique structural features that make it stand out in the realm of organic chemistry.
Structural Characteristics
- It has a linear carbon chain with multiple double bonds, giving it a distinctive reactivity.
- The presence of the ketone functional group (C=O) contributes to its interesting chemical properties.
- As indicated by its name, this compound has dimethyl substitutions which can influence its physical and chemical behavior.
Chemical Properties
This compound showcases some intriguing chemical behavior:
- Due to its unsaturated structure, it can engage in addition reactions that transform its double bonds.
- It may also participate in cross-coupling reactions, which are of great interest in the field of synthetic organic chemistry.
- The ketone group allows for oxidation reactions that can lead to various derivative compounds.
Applications and Uses
2,6-Dimethylhepta-2,5-dien-4-one has potential applications across various fields:
- It can be utilized in the development of fragrances and flavors in the food and cosmetic industries.
- Researchers are investigating its use as a starting material for the synthesis of more complex molecules.
- Its unique structure may make it insightful in mechanistic studies of organic reactions.
A Unique Compound in Research
In the ongoing quest to create new materials and understand chemical reactivity, 2,6-dimethylhepta-2,5-dien-4-one serves as a model compound. Its complex structure and reactivity profile provide a rich area for exploration and learning in both academic and industrial settings.
Synonyms
2,6-Dimethyl-2,5-heptadien-4-one
504-20-1
PHORONE
2,6-Dimethylhepta-2,5-dien-4-one
Diisopropylidene acetone
Foron
Diisobutenyl ketone
2,5-Heptadien-4-one, 2,6-dimethyl-
Phoron
Phoron [German]
s-Diisopropylidene acetone
diisopropylideneacetone
sym-Diisopropylidene acetone
NSC 38718
CCRIS 4350
EINECS 207-986-3
8F20OEI0MV
BRN 1699751
DTXSID1021584
CHEBI:35572
AI3-00047
PHORONE [MI]
NSC-38718
DTXCID101584
4-01-00-03564 (Beilstein Handbook Reference)
symDiisopropylidene acetone
2,6Dimethyl2,5heptadien4one
2,6Dimethylhepta2,5dien4one
2,5Heptadien4one, 2,6dimethyl
207-986-3
2,6-dimethyl-hepta-2,5-dien-4-one
2,6-Dimethyl-2,5-heptadiene-4-one
MFCD00008901
2,5-heptadien-4-one
WLN: 1Y1&U1V1UY1&1
UNII-8F20OEI0MV
Diisobutenylketone
SCHEMBL157728
CHEMBL2766015
NSC38718
Tox21_201097
BBL100361
NSC403517
STL554155
AKOS015841777
CS-W018571
FD33562
GS-4453
NSC-403517
NCGC00248921-01
NCGC00258649-01
2 pound not6-dimethyl-5-heptadien-4-one
AC-37908
CAS-504-20-1
SY026937
DB-116500
2,6-Dimethyl-2,5-heptadien-4-one, 95%
NS00022246
2,6-DIMETHYL-2,5-HEPTADIEEN-4-ONE
EN300-125149
F12420
Q612199
InChI=1/C9H14O/c1-7(2)5-9(10)6-8(3)4/h5-6H,1-4H
2,6-Dimethylhepta-2,5-dien-4-one; Phorone; 2,6-Dimethyl-2,5-heptadien-4-one
Solubility of 2,6-dimethylhepta-2,5-dien-4-one
2,6-dimethylhepta-2,5-dien-4-one, with its unique structure, presents a fascinating profile regarding solubility. This compound is largely non-polar due to the presence of multiple carbon atoms within the carbon chain. As a result, it exhibits a distinctive pattern in its interaction with solvents.
In terms of solubility:
In summary, the solubility behavior of 2,6-dimethylhepta-2,5-dien-4-one can be encapsulated by the idea that “like dissolves like.” Its non-polar nature steers it toward solubility in non-polar environments, making it an intriguing component for various organic reactions.