Interesting facts
Interesting Facts about 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene is a fascinating compound that presents unique structural and chemical characteristics. Here are some intriguing facts about this compound:
- Structural Complexity: This compound features a bicyclic structure, meaning it consists of two interconnected rings. The "bicyclo" prefix indicates the compound's distinct geometry, which contributes to its stability and reactivity.
- Stereochemistry: The positioning of the substituents on the rings adds a layer of stereochemical intricacy. The presence of three methyl groups at specific positions enhances the compound's steric bulk, influencing its properties and potential reactions.
- Role in Organic Synthesis: 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene serves as an important intermediate in organic synthesis. Its unique structure allows chemists to create various derivatives that can be applied in different fields, including pharmaceuticals and agrochemicals.
- Natural Occurrence: Compounds with similar structures can often be found in nature. They may occur as constituents of plant oils and give rise to various aromas and flavors, highlighting their importance in natural product chemistry.
As a compound that embodies *both structural elegance* and *synthetic utility*, 2,6,6-trimethylbicyclo[3.1.1]hept-2-ene continues to be a subject of interest among chemists. It challenges the imagination, offering a platform for exploring various chemical transformations and applications.
In conclusion, the uniqueness of this compound lies in its ability to bridge the gap between structure and function, making it a prime candidate for further study in organic chemistry.
Synonyms
ALPHA-PINENE
80-56-8
2-Pinene
Acintene A
.alpha.-Pinene
2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
pin-2(3)-ene
Pinene isomer
alfa-Pinene
Sylvapine A
PINENE, ALPHA
2437-95-8
(+/-)-alpha-Pinene
(+/-)-2-Pinene
NSC 7727
pin-2-ene
Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-
Leavo-95
DTXSID4026501
CHEBI:36740
(+-)-2-pinene
NSC-7727
2,6,6-Trimethylbicyclo(3.1.1)-2-hept-2-ene
PC-500(TERPENE)
FEMA No. 2902
alpha-Pinene (natural)
FEMA Number 2902
DTXCID006501
4,6,6-Trimethylbicyklo(3,1,1)hept-3-en
2,6,6-Trimethylbicyclo(3.1.1)hept-2-ene
(1S)-(-)-alpha-Pinene
NSC94522
NSC94523
CCRIS 697
PC-500
HSDB 720
NCGC00090682-01
(-)-?-Pinene
DL-Pin-2(3)-ene
EINECS 201-291-9
EINECS 219-445-9
UNII-JPF3YI7O34
BRN 3194807
(1R)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
AI3-24594
Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl
1S-.alpha.-Pinene
CAS-80-56-8
2,6,6-Trimethylbicyclo(3.1.1)-2-heptene
2,6,6-Trimethylbicyclo[3.1.1]-2-heptene
EC 201-291-9
(1S)-(-)-a-Pinene
4-05-00-00456 (Beilstein Handbook Reference)
alphapinene
alpha pinene
an alpha-pinene
Cyclic dexadiene
alpha -pinene
alpha.-pinene
4,6,6-trimethylbicyclo[3.1.1]hept-3-ene
Acitene A
(-)alpha-pinene
a-Pinene PF
Pinene, .alpha.
alpha [D] Pinene
alpha [L] Pinene
AUSTRALENE
(+-)-alpha-pinene
1R-.alpha.-Pinene
(R)-.alpha.-Pinene
PINENE (ALPHA)
? PINENE
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
PINENE, ALPHA (D)
PINENE, ALPHA (L)
Pesticide Code: 067004.
(.+/-.)-.alpha.-Pinene
alpha-PINENE, (+/-)-
CHEMBL442565
NSC7727
alpha-Pinene (+/-)-alpha-Pinene
Tox21_110996
Tox21_200108
Tox21_303385
NSC-94522
NSC-94523
PC 500
AKOS000121239
AB86235
AB86464
AB93066
DB15573
UN 2368
NCGC00090682-02
NCGC00257379-01
NCGC00257662-01
FP158530
LS-13835
Trimethyl Bicyclo (3.1.1) hept-2-ene
2,6-Trimethylbicyclo[3.1.1]-2-heptene
DB-017892
Bicyclo[3.1.1]hept-2-ene,6,6-trimethyl-
NS00067073
2,6-Trimethylbicyclo[3.1.1]-2-hept-2-ene
EN300-21685
C09880
Q27104380
2,6,6-TRIMETHYLBICYCLO (3.1.1)HEPT-2-ENE, 9CL
BICYCLO(3.1.1)HEPT-2-ENE,2,6,6-TRIMETHYL-2-PINENE
Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (.+/-.)-
(+/-)-2-Pinene, 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene, alpha-Pinene
201-291-9
Solubility of 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene is a fascinating compound with specific solubility characteristics that merit attention. As an organic compound, its solubility behavior is influenced by its non-polar nature, largely due to the presence of multiple carbon and hydrogen atoms. Here are some key points regarding its solubility:
Overall, the solubility of 2,6,6-trimethylbicyclo[3.1.1]hept-2-ene emphasizes the significance of polarity in organic chemistry, highlighting that "like dissolves like." This principle underscores the challenge of dissolving non-polar compounds in polar environments, thereby guiding practical applications in the chemical industry.