CAS 20267-93-0
:(1-hydroxy-4-oxido-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl)methyl 2,3-dihydroxy-2-(propan-2-yl)butanoate
Description:
The chemical substance known as "(1-hydroxy-4-oxido-2,3,5,7a-tetrahydro-1H-pyrrolizin-7-yl)methyl 2,3-dihydroxy-2-(propan-2-yl)butanoate," with the CAS number 20267-93-0, is a complex organic compound characterized by its unique structural features. It contains a pyrrolizin ring, which contributes to its cyclic nature and potential biological activity. The presence of multiple hydroxyl groups indicates that it may exhibit significant polarity, influencing its solubility and reactivity. The ester functional group, derived from the butanoate moiety, suggests potential for esterification reactions and interactions with biological systems. This compound may also display chiral properties due to the presence of asymmetric carbon centers, which can affect its pharmacological profile. Overall, its intricate structure suggests potential applications in medicinal chemistry, particularly in the development of bioactive compounds, though specific biological activities would require further investigation through empirical studies.
Formula:C15H25NO6
InChI:InChI=1/C15H25NO6/c1-9(2)15(20,10(3)17)14(19)22-8-11-4-6-16(21)7-5-12(18)13(11)16/h4,9-10,12-13,17-18,20H,5-8H2,1-3H3
SMILES:CC(C)C(C(C)O)(C(=O)OCC1=CCN2(=O)CCC(C12)O)O
Synonyms:- Butanoic acid, 2,3-dihydroxy-2-(1-methylethyl)-, (2,3,5,7a-tetrahydro-1-hydroxy-4-oxido-1H-pyrrolizin-7-yl)methyl ester
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
Echinatine N-oxide
CAS:Echinatine N-oxide is a natural product for research related to life sciences. The catalog number is TN3915 and the CAS number is 20267-93-0.Formula:C15H25NO6Purity:98%Color and Shape:SolidMolecular weight:315.36Echinatine n-oxide
CAS:Natural alkaloidFormula:C15H25NO6Purity:≥ 95.0 % (HPLC)Color and Shape:SolidMolecular weight:315.36Echinatine N-oxide
CAS:Echinatine N-oxide is an alkaloid compound, which is a natural product derived from certain plant species belonging to the Acanthaceae family. As a metabolite, it is synthesized by these plants as part of their secondary metabolite pathways. Its mode of action is thought to involve interaction with biological macromolecules through its oxygenated nitrogen group, which may affect various biochemical pathways.Formula:C15H25NO6Purity:Min. 95%Molecular weight:315.36 g/molRef: 4Z-E-191002
Discontinued product





