Interesting facts
Interesting Facts about 2,6,6-Trimethylnorpinane
2,6,6-trimethylnorpinane is a fascinating organic compound that falls under the category of bicyclic hydrocarbons. Its unique structure and properties offer various points of interest for chemists and chemical enthusiasts alike. Here are some engaging facts about this compound:
- Structural Complexity: 2,6,6-trimethylnorpinane features a bicyclic framework, which means it contains two linked rings in its structure. This complexity can affect its reactivity and interactions with other molecules, making it a subject of study in organic chemistry.
- Synthesis: The synthesis of 2,6,6-trimethylnorpinane often involves intricate methods that can include cyclization reactions and functional group modifications. This presents an excellent opportunity for students to explore practical applications and techniques in synthetic organic chemistry.
- Natural Occurrence: This compound may be found in trace amounts in various natural sources, which can be intriguing for those studying natural products or terpenes. Identifying and isolating such compounds from nature is a captivating endeavor for chemists.
- Potential Applications: While 2,6,6-trimethylnorpinane may not be widely known, compounds with similar bicyclic structures are often explored for their potential use in pharmaceuticals, agrochemicals, and perfumes. Understanding its properties could lead to new applications in these areas.
- Research Opportunities: Due to its interesting structure, 2,6,6-trimethylnorpinane can be a model compound for studying stereochemistry, conformation, and ring strain, providing rich ground for academic inquiry and research projects.
In summary, 2,6,6-trimethylnorpinane exemplifies the vast diversity found in organic chemistry. Its structural intricacies and potential applications make it an intriguing subject for both scholars and learners in the field.
Synonyms
Pinane
473-55-2
2,6,6-Trimethylbicyclo[3.1.1]heptane
DIHYDROPINENE
Bicyclo[3.1.1]heptane, 2,6,6-trimethyl-
HSDB 5664
EINECS 207-467-1
Bicyclo(3.1.1)heptane, 2,6,6-trimethyl-
NSC 76674
2,6,6-Trimethylbicyclo(3.1.1)heptane
DTXSID7025922
UNII-140V20YT81
CHEBI:35710
1a,2b,5a-2,6,6-Trimethylbicyclo(3.1.1)heptane
DTXCID705922
NSC-76674
2,6,6-trimethylbicyclo(3.1.1)heptane;pinane
2,6,6-trimethylbicyclo[3.1.1]heptane;pinane
Pinane (8CI)
DIHYDROPINENE [HSDB]
2,6,6Trimethylbicyclo(3.1.1)heptane
Bicyclo(3.1.1)heptane, 2,6,6trimethyl
1a,2b,5a2,6,6Trimethylbicyclo(3.1.1)heptane
2,6,6-TRIMETHYLBICYCLO(3,1,1)HEPTANE
2,7,7-TRIMETHYLBICYCLO(3.1.1)HEPTANE
(1s,2s,5s)-2,6,6-trimethylbicyclo(3.1.1)heptane
inchi=1/c7h12/c1-2-6-4-7(3-1)5-6/h6-7h,1-5h
un3295
Pinane, endo + exo
(1S)-(-)-trans-Pinane
PINANE (2-D1)
PINANE (3-D1)
6876-13-7
CAS-473-55-2
Pinane, didehydro derivative
Caswell No. 664
NCIOpen2_000688
UNII-996299PUKB
CHEMBL1422299
996299PUKB
NSC76674
EINECS 215-533-6
Tox21_202039
Tox21_303280
2,6-Trimethylbicyclo[3.1.1]heptane
AKOS015960556
AKOS037643346
140V20YT81
EPA Pesticide Chemical Code 067001
Bicyclo[3.1.1]heptane,6,6-trimethyl-
NCGC00090847-01
NCGC00090847-02
NCGC00257210-01
NCGC00259588-01
AS-14849
LS-13860
2,6,6-Trimethylbicyclo[3.1.1]heptane #
DB-329663
NS00077419
E75920
Q2095373
Bicyclo(3.1.1)heptane, 2,6,6-trimethyl-, didehydro deriv.
Bicyclo[3.1.1]heptane, 2,6,6-trimethyl-, [1R-(1.alpha.,2.beta.,5.alpha.)]-
Solubility of 2,6,6-Trimethylnorpinane
2,6,6-Trimethylnorpinane, with the chemical formula C15H26, exhibits some interesting properties regarding its solubility. Due to its predominantly hydrocarbon structure, this compound is:
This behavior is typical for compounds primarily composed of carbon and hydrogen, reflecting the principle that "like dissolves like." The overall molecular structure contributes to its solubility characteristics, making it a compound best suited for organic-based environments.