CAS 1465-77-6
:7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2,3-dimethyl-, sodium salt (1:2), (1R,2S,3R,4S)-rel-
Description:
7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2,3-dimethyl-, sodium salt (1:2), (1R,2S,3R,4S)-rel- is a chemical compound characterized by its bicyclic structure, which includes a seven-membered ring containing an oxygen atom. This compound features two carboxylic acid functional groups, contributing to its acidity and potential reactivity. The presence of two methyl groups at the 2 and 3 positions of the bicyclic framework influences its steric and electronic properties, potentially enhancing solubility and reactivity in various chemical environments. As a sodium salt, it is likely to exhibit increased solubility in aqueous solutions compared to its acid form. The specific stereochemistry indicated by the (1R,2S,3R,4S) configuration suggests that the compound has defined spatial arrangements of its substituents, which can significantly affect its biological activity and interactions. Overall, this compound may find applications in organic synthesis, pharmaceuticals, or as a biochemical reagent, although specific applications would depend on further research and characterization.
Formula:C10H14O5·2Na
InChI:InChI=1/C10H14O5.2Na/c1-9(7(11)12)5-3-4-6(15-5)10(9,2)8(13)14;;/h5-6H,3-4H2,1-2H3,(H,11,12)(H,13,14);;/t5-,6+,9+,10-;;
InChI key:InChIKey=WHKZSDQWVMLPNE-CSYCBQNYNA-N
SMILES:C(O)(=O)[C@@]1(C)[C@](C(O)=O)(C)[C@]2(O[C@@]1(CC2)[H])[H].[Na]
Synonyms:- 7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2,3-dimethyl-, disodium salt
- Disodium cantharidin
- 7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2,3-dimethyl-, sodium salt (1:2), (1R,2S,3R,4S)-rel-
- 7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2,3-dimethyl-, disodium salt, (1R,2S,3R,4S)-rel-
- 7-Oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid, 2,3-dimethyl-, disodium salt, (exo,exo)-
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Found 1 products.
Cantharidic acid
CAS:<p>Cantharidic acid is an anticancer agent that inhibits the energy metabolism of cancer cells by inhibiting the activity of key enzymes, such as phosphatase and cyclase. It has been shown to be effective in inducing antibody response in mice and reducing the number of regulatory T-cells. Cantharidic acid also induces apoptosis through a regulatory element, which may be responsible for the potent immunosuppressive effects of cantharidic acid. Clinical studies have found cantharidic acid to be effective against infectious diseases caused by bacteria, such as Salmonella and Staphylococcus.</p>Formula:C10H12Na2O5Purity:Min. 95%Molecular weight:258.18 g/mol
