Interesting facts
Interesting Facts About 7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic Acid
7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid is a fascinating compound that has garnered attention in the fields of synthetic chemistry and pharmaceuticals. Here are some intriguing aspects of this compound:
- Unique Structure: The molecule features a bicyclic framework that is rare in organic chemistry, presenting a bridged structure with two carboxylic acid groups. This unique architecture can influence its reactivity and function in various chemical reactions.
- Potential Applications: Due to its structural properties, 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid has been investigated for use in drug development, particularly as a potential scaffold for designing novel pharmaceuticals.
- Environmental Impact: Research suggests that derivatives of this compound may possess biodegradable properties, making them suitable candidates for environmentally friendly materials in various applications.
- Synthetic Routes: Several synthetic pathways have been developed to produce this compound, including cycloaddition and ring-opening reactions, which showcase the versatility of synthetic organic chemistry.
- Comparative Studies: Scientists often perform comparisons between this compound and other dicarboxylic acids to explore differences in reactivity, solubility, and biological activity, which can yield insights into their functional potential.
- Hydrophilicity: The presence of two carboxylic acid groups contributes to the compound's hydrophilic character, allowing it to interact well with other polar molecules, which is especially relevant in biochemical contexts.
As the field of chemical research continues to advance, compounds like 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid exemplify the remarkable diversity and utility within organic compounds, paving the way for innovative discoveries.
Synonyms
endothall
Endothal
7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid
145-73-3
Tri-Endothal
Hydrothal-47
Hydrothal-191
Aquathol
Endothal technical
3,6-endo-Oxohexahydrophthalic acid
RCRA waste number P088
3,6-endo-Oxyphthalic acid hexahydro-
DTXSID7024081
NSC237771
NSC 112771
Phthalic acid, hexahydro-3,6-endo-oxy-
28874-46-6
CAS-145-73-3
DTXCID204081
Niagrathal
7-Oxabicyclo(2.2.1)heptane-2,3-dicarboxylic acid, (1R,2S,3R,4S)-rel-
1, 3,6-endo-epoxy-
Phthalic acid,6-endo-oxy-
CHEMBL8080
Lopac0_000542
SCHEMBL55158
BMK1-H1
1, hexahydro-3,6-endo-oxy-
WLN: T55 A AOTJ CVQ DVQ
Tox21_202446
Tox21_300094
HSCI1_000365
NSC112771
AKOS024418784
CCG-204632
HY-113976A
NSC-237771
NCGC00015419-02
NCGC00015419-03
NCGC00015419-04
NCGC00015419-05
NCGC00015419-06
NCGC00015419-07
NCGC00093930-01
NCGC00093930-02
NCGC00254025-01
NCGC00259995-01
MS-23003
DB-042801
CS-0086309
EU-0100542
NS00015678
D85116
E 7649
SR-01000075864
Q3054030
SR-01000075864-1
Solubility of 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid
7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, with the chemical formula C8H10O5, exhibits noteworthy solubility characteristics influenced by its functional groups. This compound contains two carboxylic acid groups, which significantly enhance its ability to dissolve in polar solvents.
The solubility of 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid can be summarized as follows:
Overall, the solubility of 7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid is a function of its molecular structure and the nature of the solvent, emphasizing the importance of functional groups in determining solubility.