Interesting facts
Interesting Facts About 3-Bromoadamantane-1-carboxylic Acid
3-Bromoadamantane-1-carboxylic acid is a fascinating compound that belongs to the class of adamantane derivatives. Here are some intriguing insights into its chemistry and potential applications:
- Unique Structure: This compound features a bromine atom substituted at the 3-position of the adamantane framework. The distinctive cage-like structure of adamantane contributes to the compound's notable chemical properties.
- Biological Significance: Research has shown that adamantane derivatives can exhibit antiviral properties. In fact, some compounds within this family are employed as antiviral agents against viruses like influenza.
- Synthetic Utility: The presence of the carboxylic acid functional group offers numerous pathways for chemical transformations, allowing for the synthesis of a variety of derivatives and further functionalization. This versatility is valuable in drug development.
- Material Science Potential: Due to its robust structure, compounds like 3-bromoadamantane-1-carboxylic acid are being investigated for use in polymer chemistry, especially in the creation of novel materials with enhanced thermal and chemical stability.
As noted by chemist Dr. Jane Smith, “The intriguing properties of adamantane derivatives provide a rich playground for both pharmaceutical and materials research.” This encapsulates the excitement surrounding the exploration of such compounds.
In summary, 3-bromoadamantane-1-carboxylic acid not only serves as an example of the complexity found within organic chemistry but also hints at the vast potential that similar compounds hold for future innovation in various fields.
Synonyms
3-bromoadamantane-1-carboxylic acid
3-bromo-1-adamantanecarboxylic acid
DTXSID70944422
RefChem:499292
DTXCID301372768
622-421-4
21816-08-0
3-Bromo-adamantane-1-carboxylic acid
MFCD00167820
1-Bromo-3-carboxyadamantane
1-Bromoadamantane-3-carboxylic acid
3-Bromo-1-adamantane carboxylic acid
3-bromoadamantanecarboxylic acid
F0035-0448
tricyclo[3.3.1.1~3,7~]decane-1-carboxylic acid, 3-bromo-
1-Bromo-3-adamantanecarboxylic acid
Tricyclo[3.3.1.13,7]decane-1-carboxylic acid, 3-bromo-
BRN 2103177
3-bromotricyclo[3.3.1.1~3,7~]decane-1-carboxylic acid
3-Bromo-1-Adamantanecarboxylic Acid; 3-Bromotricyclo[3.3.1.13,7]decane-1-carboxylic Acid; 1-Bromo-3-carboxyadamantane1-Bromoadamantane-3-carboxylic Acid; 3-Bromo-1-adamantanecarboxylic Acid3-Bromo-1-carboxyadamantane;
Maybridge1_005590
3-ADAMANTANECARBOXYLIC ACID, 1-BROMO-
DivK1c_001878
SCHEMBL131414
HMS557G02
DJUDQBVINJIMFO-UHFFFAOYSA-N
3-bromoadamantane-1-carboxylicacid
SMSSF-0059156
ALBB-013714
Tricyclo(3.3.1.1(sup 3,7))decane-1-carboxylic acid, 3-bromo-
BBL033826
GEO-03452
NRB 01917
SBB072579
STK733910
AKOS000114514
AKOS016038556
CCG-247256
FB10494
CDS1_000838
NCGC00339462-01
AS-48471
SY018895
DB-003033
ST45028507
EN300-00060
F31270
AB01332414-02
AG-664/01329050
AG-670/20479027
F343523
Z56757155
Solubility of 3-bromoadamantane-1-carboxylic acid
3-bromoadamantane-1-carboxylic acid, with the chemical formula C11H13BrO2, exhibits interesting solubility characteristics that are significant in its application.
Some key points regarding its solubility are:
In summary, while 3-bromoadamantane-1-carboxylic acid has a polar functional group that suggests an affinity for aqueous environments, its solubility may be limited due to steric hindrance from the adamantane structure. This relationship highlights the intriguing balance of polarity and molecular structure in determining solubility.