Interesting facts
Interesting Facts about 3-Methylcyclohex-2-en-1-one
3-Methylcyclohex-2-en-1-one is quite an intriguing compound with various applications and properties that can capture the interest of both scientists and chemistry students alike. Here are some fascinating aspects to consider:
- Structural Characteristics: This compound features a unique ring structure that includes a double bond and a ketone functional group, making it a part of the larger family of cyclic compounds.
- Natural Occurrence: 3-Methylcyclohex-2-en-1-one is not merely an abstract concept found in laboratories; it can be found in certain natural products, often contributing to the aroma and flavor of various essential oils.
- Synthesis: The compound can be synthesized through various organic reactions, such as the hydroformylation of alkynes or through other innovative synthetic routes, showcasing the creativity involved in organic chemistry.
- Applications: Its reactivity lends itself to a range of applications in the creation of >flavoring agents, fragrances, and even pharmaceuticals, illustrating the practical side of studying organic compounds.
- Stability Considerations: The presence of the double bond in the cyclohexene structure can often lead to interesting stability and reactivity profiles, making it a valuable subject of study in reaction mechanisms.
In the words of chemist Robert H. Grubbs, "Chemistry is not about atoms and molecules, but about understanding the interactions that allow them to create the complexity we observe in nature." This compound certainly embodies that idea, serving as a bridge between theoretical study and real-world applications.
As you delve deeper into the study of 3-methylcyclohex-2-en-1-one, you may find yourself inspired by its multifunctional nature and the myriad of ways it can contribute to advancements in science and industry.
Synonyms
3-METHYL-2-CYCLOHEXEN-1-ONE
3-Methylcyclohex-2-en-1-one
3-Methyl-2-cyclohexenone
Seudenone
2-Cyclohexen-1-one, 3-methyl-
Methylcyclohexenone
Caswell No. 561AB
FEMA No. 3360
nutty cyclohexenone
3-Methyl-2-cyclohexene-1-one
EINECS 214-769-7
NSC 43632
ghl.PD_Mitscher_leg0.699
EPA Pesticide Chemical Code 219700
BRN 1560601
DTXSID8035186
UNII-786Y352V9X
AI3-19937
NSC-43632
786Y352V9X
3-Methyl-2-cyclohexenone-1
DTXCID6015186
FEMA 3360
4-07-00-00130 (Beilstein Handbook Reference)
3-METHYL-2-CYCLOHEXEN-1-ONE [FHFI]
MCH CPD
3-Methyl-D2-cyclohexenone
iitqjmyaysnimi-uhfffaoysa-n
inchi=1/c7h10o/c1-6-3-2-4-7(8)5-6/h5h,2-4h2,1h
1193-18-6
MFCD00001581
3-methyl-cyclohex-2-en-1-one
CHEBI:88428
3-Methylcyclohexenone
3-methyl-cyclohexenone
3-methylcyclohex-2-enone
3-methyl-cyclohex-2-enone
SCHEMBL124901
CHEMBL3139347
3-Methyl-2-cyclohexenone, 98%
NSC43632
Tox21_302036
AKOS004909936
AKOS025243221
FM35625
s10448
NCGC00255585-01
NS-00067
SY011435
CAS-1193-18-6
DB-041462
CS-0128362
M1043
NS00020937
EN300-66416
3-Methyl-2-cyclohexenone, >=98%, stabilized, FG
Q27160291
Z1042078386
Solubility of 3-Methylcyclohex-2-en-1-one
3-Methylcyclohex-2-en-1-one, a compound characterized by its unique cyclic structure and unsaturated carbonyl group, exhibits interesting solubility properties that are worth exploring. This compound is largely soluble in organic solvents due to its hydrophobic cyclohexane ring and the presence of a polar carbonyl group. Here are a few key points regarding its solubility:
In summary, while 3-methylcyclohex-2-en-1-one is not soluble in water, its compatibility with various organic solvents enhances its utility in chemical applications. Understanding solubility is crucial for effective usage in synthesis and reaction mechanisms.