Interesting facts
Interesting Facts about 4-Isopropenylcyclohexene-1-carboxylic Acid
4-Isopropenylcyclohexene-1-carboxylic acid is a fascinating organic compound that draws interest due to its unique structure and potential applications in various fields of chemistry and materials science. Below are several noteworthy aspects of this compound:
- Reactivity: The presence of the isopropenyl group in its structure makes this compound highly reactive, allowing it to participate in various chemical reactions, such as Diels-Alder reactions and Michael additions, which can be exploited in organic synthesis.
- Potential Applications: Due to its ability to undergo polymerization, 4-isopropenylcyclohexene-1-carboxylic acid is of interest for use in creating coatings and adhesives that require specific properties like flexibility and durability.
- Natural Product Derivative: This compound serves as a structural mimic of certain natural products, which may pave the way for the synthesis of novel pharmaceuticals, particularly those targeting specific biological pathways.
- Analytical Importance: Its distinctive functional groups make it invaluable for analytical chemists who seek to develop new methods for isolating and identifying similar compounds found in natural sources.
- Environmental Considerations: As regulations become stricter surrounding the use of synthetic chemicals, investigating compounds like 4-isopropenylcyclohexene-1-carboxylic acid may lead to more sustainable and eco-friendly alternatives in industrial applications.
In conclusion, 4-isopropenylcyclohexene-1-carboxylic acid represents a bridge between fundamental research and practical applications, showcasing the essential role of organic compounds in advancing technology and innovation. As one researcher aptly stated, "The true beauty of chemistry lies in the connections and reactions we can harness to create something entirely new."
Synonyms
Perillic acid
7694-45-3
(-)-perillic acid
Perillicacid
4-Isopropenylcyclohex-1-enecarboxylic acid
4-prop-1-en-2-ylcyclohexene-1-carboxylic acid
PKS69DU4ZQ
4-(1-methylethenyl)-1-cyclohexene-1-carboxylic acid
1-Cyclohexene-1-carboxylicacid, 4-(1-methylethenyl)-
CHEBI:36999
4-Isopropenyl-1-cyclohexene-1-carboxylic acid
4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic acid
1-Cyclohexene-1-carboxylic acid, 4-(1-methylethenyl)-
SR-01000076076
EINECS 231-709-5
4-isopropenylcyclohex-1-ene carboxylic acid
4-(2-propenyl)-1-cyclohexane-1-carboxylic acid
UNII-PKS69DU4ZQ
Lopac0_001001
SCHEMBL465998
CHEMBL1373981
DTXSID60864105
HMS3263I03
Tox21_501001
NSC641067
AKOS006230667
CCG-205081
LMPR0102090041
LP01001
NSC-641067
SDCCGSBI-0050974.P002
NCGC00015832-02
NCGC00015832-03
NCGC00015832-04
NCGC00015832-05
NCGC00015832-06
NCGC00015832-07
NCGC00094295-01
NCGC00094295-02
NCGC00094295-03
NCGC00094295-04
NCGC00261686-01
NCI60_013759
SY316382
HY-113471
CS-0062325
EU-0101001
NS00015181
P 7083
SR-01000076076-1
SR-01000076076-5
SR-01000076076-6
(S)-4-(1-Propen-2-yl)cyclohex-1-enecarboxylic Acid
Q27104388
1A4758DA-6365-4FD5-BAEA-16032D3488FF
Solubility of 4-isopropenylcyclohexene-1-carboxylic acid
4-isopropenylcyclohexene-1-carboxylic acid (C10H14O2) is a compound that showcases interesting solubility characteristics due to its unique molecular structure. This compound can be classified as a carboxylic acid, which typically influences its solubility behavior through:
As a result, the solubility of 4-isopropenylcyclohexene-1-carboxylic acid is primarily influenced by environmental factors such as:
In summary, while 4-isopropenylcyclohexene-1-carboxylic acid exhibits a degree of solubility in polar solvents due to its functional groups, its hydrophobic cyclohexene component can limit its overall solubility in purely aqueous environments. Therefore, it may demonstrate a more favorable solubility profile in organic solvents, making it useful in various chemical applications.