Interesting facts
Interesting Facts about (7,7-Dimethyl-2-oxo-norbornan-1-yl)methanesulfonic Acid
(7,7-Dimethyl-2-oxo-norbornan-1-yl)methanesulfonic acid is a fascinating compound noteworthy for several reasons:
- Structural Complexity: The compound features a unique bicyclic structure characteristic of norbornane, which provides it with a degree of rigidity and stability that is rare in organic compounds. This could be advantageous in various synthetic applications.
- Functional Groups: It contains both a sulfonic acid group and a carbonyl group, which significantly impacts its reactivity. The sulfonic acid moiety is particularly interesting due to its ability to act as a strong acid in solutions, enabling potential use in catalysis.
- Application in Organic Synthesis: Its structural attributes make it a valuable intermediate in organic synthesis, particularly in the design of pharmaceuticals and agrochemicals. As scientists strive for more sustainable synthesis methods, compounds like this can serve as platform chemicals.
- Biological Relevance: Compounds related to methanesulfonic acid have been studied for their biological activities. Understanding their mechanism of action could reveal important insights into medicinal chemistry.
Additionally, the study of (7,7-dimethyl-2-oxo-norbornan-1-yl)methanesulfonic acid provides an excellent opportunity for students and researchers to explore:
- Reaction Mechanisms: Investigating how this compound participates in various chemical reactions enhances one's understanding of organic reaction mechanisms.
- Analytical Techniques: Analyzing the compound can enhance skills in modern analytical chemistry methods, such as NMR, HPLC, and mass spectrometry.
- Intermolecular Interactions: This compound can serve as a model for studying intermolecular forces, impacting solubility, reactivity, and physical properties.
In summary, (7,7-dimethyl-2-oxo-norbornan-1-yl)methanesulfonic acid is more than just a chemical formula; it is a gateway to discovering the rich and intricate world of organic chemistry.
Synonyms
Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-
Bicyclo(2.2.1)heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-
5872-08-2
CAMPHORSULFONIC ACID
(7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonic acid
DL-10-Camphorsulfonic acid
61380-66-3
camphor sulfonic acid
d-10-Camphorsulfonic acid
(7,7-dimethyl-2-oxo-1-bicyclo[2.2.1]heptanyl)methanesulfonic acid
DL-CAMPHORSULFONIC ACID
(+)-10-CAMPHORSULFONIC ACID
(+)-Camphorsulfonic acid
D-Camphor-10-sulfonic acid
7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonic acid
(+/-)-10-Camphorsulfonic Acid
L-10-(-)-Camphor sulfonic acid
(+/-)-Camphor-10-sulfonic acid
( inverted exclamation markA)-Camphor-10-sulfonic acid
10-CSA
(+)-Camphor-10-sulfonic acid
L-(+)-CAMPHORSULFONICACID
{7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl}methanesulfonic acid
(+)-CSA
(1S)-(+)-10-Camphorsulfonic acid
L-Camphor-10-sulfonic acid
10-Camphorsulfonic acid
1R-(-)-Camphorsulfonic acid
(+/-)-camphorsulfonic acid
dl-camphor sulfonic acid
L-(+)-CAMPHORSULFONIC ACID
s-(+)-camphor sulfonic acid
(1S)-(+)-Camphor-10-sulfonic acid(dry wt.),water
76-26-6
(-)-CSA
Camsylate
MFCD00064157
Camphersulfonsaure
(1S)-(+)-Camphor-10-sulfonic acid
camphorsulphonic acid
camphor sulphonic acid
(-)camphorsulfonic acid
10-camphorsulphonic acid
(+) camphorsulfonic acid
(+)camphor sulfonic acid
(-) camphorsulfonic acid
10-camphor sulfonic acid
camphor-10-sulphonic acid
(rac)-Camphorsulfonic acid
SCHEMBL3604
(+)-10camphorsulfonic acid
(+/-) camphorsulfonic acid
(+/-) camphor sulfonic acid
Dextro-10-camphorsulfonic acid
(-)-10-camphorsulphonic acid
(+)-Camphor-10-sulphonic acid
CHEBI:55379
(-/+)-10-camphorsulfonic acid
DTXSID60863113
racemic camphor-10-sulfonic acid
(+)-.beta.-Camphorsulfonic acid
(+/-)-10-camphorsulphonic acid
(+/-)-10-camphor sulfonic acid
Camphor-10-sulfonic acid, (+)-
(+/-) 10-camphor sulphonic acid
CS-D1796
(+/-)-CSA
(7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonicacid
.beta.-Camphorsulfonic acid, (+)-
Camphor-10-sulfonic acid ( beta )
STL490650
(s)-(+)-camphor-10-sulphonic acid
AKOS000267736
AKOS016039123
Camphor-.omega.-sulfonic acid, (+)-
CS-W001192
CS-W012934
FC31710
HY-W012218
AC-12238
BS-17109
(+)-Camphor-10-sulfonic acid (.beta.)
DB-016134
DB-016160
NS00041086
EN300-20050
P20541
Q414283
SR-01000944696
SR-01000944696-1
F2124-0036
Dl-oxo-10-bornanesulfonic acid;dl-camphor-10-sulfonic acid
(7,7-Dimethyl-2-oxobicyclo[2.2.1]-heptan-1-yl)methanesulfonic acid
{7,7-DIMETHYL-2-OXOBICYCLO[2.2.1]HEPTAN-1-YLMETHANESULFONIC ACID
7,7-Dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulfonic acid, (1S,4R)-
(7,7-Dimethyl-2-oxobicyclo[2.2.1]hept-1-yl)methanesulfonic acid, (1S,4R)- #
(+/-)-7,7-Dimethyl-2-oxo-bicyclo[2.2.1]heptane-1-methanesulfonic acid;Voriconazole Related Compound F;(+/-)-10-Camphorsulfonic acid
Solubility of (7,7-dimethyl-2-oxo-norbornan-1-yl)methanesulfonic acid
(7,7-dimethyl-2-oxo-norbornan-1-yl)methanesulfonic acid is a compound that exhibits intriguing solubility characteristics. Its solubility can be influenced by various factors such as temperature and the polarity of the solvent.
When considering its solubility, here are some key points to keep in mind:
However, since this compound's solubility hasn't been extensively documented in the literature, empirical testing in various solvents is essential for precise determination. One could hypothesize, based on its structure, that solubility would be favorable in environments where the acid can ionize. It’s essential to note that the solubility behavior might differ significantly in nonpolar solvents due to the compound's structural characteristics.
In summary, while (7,7-dimethyl-2-oxo-norbornan-1-yl)methanesulfonic acid shows potential for good solubility in polar environments, experimental validation remains crucial to fully understand its solubility profile.