Interesting facts
Interesting Facts about 2,2-Dimethyl-3-methylene-norbornane
2,2-Dimethyl-3-methylene-norbornane is an intriguing compound in the family of bicyclic hydrocarbons. This organic structure is often explored through various branches of organic chemistry due to its unique framework and potential applications. Here are some fascinating insights about this compound:
- Structural Diversity: As a norbornane derivative, 2,2-dimethyl-3-methylene-norbornane exhibits a complex and unique structural arrangement. Its bicyclic arrangement provides opportunities for interesting stereochemistry, which can have significant implications in chemical reactions.
- Reactivity: The presence of the methylene group contributes to its reactivity, particularly in cycloaddition and substitution reactions. This reactivity can be harnessed in synthetic organic chemistry for the development of more complex molecules.
- Applications: Compounds like 2,2-dimethyl-3-methylene-norbornane are often valuable in the design of new materials and polymers. Their rigid structure can enhance the physical properties of polymers, leading to innovations in materials science.
- Natural Occurrence: While 2,2-dimethyl-3-methylene-norbornane may not be widely found in nature, its structural relatives can be found in various natural products, including certain terpenes. This shows a connection to biochemistry and natural product synthesis.
- Research Focus: Scientists are continually investigating norbornane derivatives to uncover potential pharmaceutical applications. The ability to modify the structure can yield compounds with desirable biological activities, making this area a rich field for research.
In conclusion, 2,2-dimethyl-3-methylene-norbornane exemplifies the richness of organic chemistry and the endless possibilities that lie within the modification of simple hydrocarbon frameworks. As chemists continue to explore its properties and applications, this compound may yet surprise us with its utility in various scientific endeavors.
Synonyms
CAMPHENE
79-92-5
Comphene
(+/-)-Camphene
2,2-Dimethyl-3-methylenenorbornane
DL-Camphene
2,2-dimethyl-3-methylidenebicyclo[2.2.1]heptane
3,3-Dimethyl-2-methylenenorbornane
3,3-Dimethyl-2-methylenenorcamphane
FEMA No. 2229
Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-
CCRIS 3783
HSDB 900
2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane
NSC 4165
3,3-Dimethyl-2-methylenenorcamphene
EINECS 201-234-8
EINECS 209-275-3
UNII-G3VG94Z26E
CHEBI:3830
G3VG94Z26E
DTXSID8026488
AI3-01775
CAMPHENE, DL-
NSC-4165
2,2-Dimethyl-3-methylenebicyclo(2.2.1)heptane
Camphene (2,2-dimethyl-3-methylene-norbornane)
Bicyclo(2.2.1)heptane, 2,2-dimethyl-3-methylene-
DTXCID006488
CAMPHENE, (+/-)-
Camphene, (1R,4S)-(+)-
EC 201-234-8
(1)-2,2-Dimethyl-3-methylenebicyclo(2.2.1)heptane
CAMPHENE (MART.)
CAMPHENE [MART.]
Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-, (1R)-
MFCD00066603
CAS-79-92-5
2,2-dimethyl-3-methylidenebicyclo(2.2.1)heptane
2,2-dimethyl-3-methylene-norbornane
CAMPHENE [FHFI]
CAMPHENE [HSDB]
CAMPHENE [FCC]
CAMPHENE [MI]
2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane #
CAMPHENE, D,L-
3,3-Dimethylenenorcamphene
CAMPHENE [WHO-DD]
Bicyclo-(2.2.1)heptane
2,2-Dimethyl-3-methylene-
3,3-dimethyl-2-methylidenebicyclo[2.2.1]heptane
CHEMBL2268550
2,2-Dimethyl-3-methylenebicyclo
NSC4165
2,2-Dimethyl-3-methylene-norborane
Tox21_202014
Tox21_303152
BBL033861
STK801857
AKOS004119935
CCG-266137
NCGC00249149-01
NCGC00257126-01
NCGC00259563-01
WLN: L55 A CYTJ CU1 D1 D1
FC145215
VS-12317
2,2-DIMETHYL-3-METHYLENE NORBORANE
DB-053130
DB-056393
DB-057848
NS00006622
3,3-DIMETHYL-2-METHYLENE NORCAMPHANE
EN300-20391
(1R,4S)-2,2-dimethyl-3-methylene-norbornane
C06076
E87135
SBI-0653924.0001
Bicyclo[2.2.1]heptane,2-dimethyl-3-methylene-
Q416775
SR-01000944833
Bicyclo(2.2.1)heptane, 2,2-dimethyl-3-methylene
SR-01000944833-1
CAMPHENE(2,2-DIMETHYL-3-METHYLENE-NORBORNANE)
Z104478010
201-234-8
Solubility of 2,2-dimethyl-3-methylene-norbornane
The solubility of 2,2-dimethyl-3-methylene-norbornane can be characterized as follows:
In summary, while 2,2-dimethyl-3-methylene-norbornane is expected to be insoluble in water, it is readily soluble in organic solvents, highlighting the importance of considering polarity when assessing solubility of organic compounds. Remember, "like dissolves like" is a mantra that often guides solubility predictions in chemistry!